Tissue repair with space-seeking spirals of filament

ABSTRACT

The distal portion of a shape-memory filament extends from a needle containing at least one filament gripping element. To implant the shape-memory filament in tissue, the needle is inserted into a cannula with a flexible and removable hook. During partial withdrawal of the needle, the hook holds the distal portion of the filament stationary to deposit a section of filament in the distal portion of the cannula. The needle is re-advanced, pushing the section of the shape-memory filament to coil or fold within the tissue. Rotation of the needle with the filament gripping element further tightens the coiled or folded filament. Partial withdrawal, re-advancement, rotation and pushing of the needle are repeated to fill, pack, strengthen, enlarge or augment the tissue with the shape-memory filament.

CROSS REFERENCE

This application is a continuation-in-part of Ser. No. 13/261,607 filedon Mar. 1, 2013, US national phase of PCT/US2012/000,158 filed on Mar.23, 2012. U.S. Provisional 61/465,804 filed on Mar. 23, 2011. U.S.Provisional 61/518,489 filed on May 7, 2011. U.S. Provisional 61/572,820filed on Jul. 21, 2011.

FIELD OF INVENTION

This invention relates to a spiraling device using filament to fill,pack and repair tissue, including intervertebral disc, urethral andfecal sphincters. The filament has a shape memory property to facilitatefilament packing in tissue.

BACKGROUND

Chronic back pain is an epidemic. Nerve impingement is not seen by CT orMRI in about 85% of back pain patients [Deyo R A, Weinstein J N: Lowback pain, N Eng J Med, 344(5) February, 363-370, 2001. Boswell M V, et.al.: Interventional Techniques: Evidence-based practice guidelines inthe management of chronic spinal pain, Pain Physician, 10:7-111, ISSN1533-3159, 2007]. In fact, lumbar disc prolapse, protrusion, orextrusion account for less than 5% of all low back problems, but are themost common causes of nerve root pain and surgical interventions(Manchikanti L, Derby R, Benyamin R M, Helm S, Hirsch J A: A systematicreview of mechanical lumbar disc decompression with nucleoplasty, PainPhysician; 12:561-572 ISSN 1533-3159, 2009). The cause of chronic backpain in most patients has been puzzling to both physicians and patients.

Studies indicate back pain is correlated with high lactic acid in thedisc. Leakage of the acid causes acid burn and persistent back pain. Inaddition, as the disc degenerates and flattens, the compressive load isshifted from the flattened disc to facet joints, causing strain andpain. Both lactic acid burn and strain of the facet joints are notvisible under CT or MRI.

Intervertebral discs are avascular (no blood vessels). Nutrients, oxygenand pH buffer 131 essential for disc cells are supplied by thecapillaries 107 in the vertebral bodies 159 and diffused from superiorand inferior endplates 105 into the disc 100, as shown in FIGS. 1 and 2.Blood pH is tightly regulated between 7.35 and 7.45, mainly by the pHbuffering bicarbonate dissolved in blood plasma diffused throughsuperior and inferior endplates 105 into the disc 100.

However, depth of diffusion is shallow into thick human discs 100. Depthof oxygen diffusion from the endplates 105 is summarized in FIG. 3(Stairmand J W, Holm S, Urban J P G: Factor influencing oxygenconcentration gradients in disc, Spine, Vol. 16, 4, 444-449, 1991).Similarly, depths of glucose diffusion are less than 3 mm from superiorand inferior endplates (Maroudas A, Stockwell R A, Nachemson A, Urban J:Factors involved in the nutrition of the human lumbar intervertebraldisc: Cellularity and diffusion of glucose in vitro, J. Anat., 120,113-130, 1975). Nearly all animals have thin discs; depths of diffusionof oxygen and nutrients seem to be sufficient. Lumbar discs of a largesheep weighing 91 kg (200 pounds) are less than 3 mm thick. However,human lumbar discs are about 7-12 mm thick. Mid layers of our thickdiscs 100 suffer severe oxygen and nutritional deficiency.

Under anaerobic condition within the mid layer, lactic acid 162 isproduced and leaked from the nucleus 128 through fissures 121 to burnsurrounding nerves 118, 194 causing persistent back pain, as depicted inFIGS. 4-6. Some patients experience leg pain without visible nerveimpingement under MRI or CT. Lactic acid 162 can leak from the nucleus128 through fissures 121 to spinal nerves 194, causing leg pain asdepicted in FIGS. 4-5. Leg pain without visible impingement is commonlycalled chemical radiculitis.

High lactic acid content in discs correlates with back pain. In fact,dense fibrous scars and adhesions, presumably from lactic acid 162 burn,can be found around nerve roots 194 during spinal surgery [Diamant B,Karisson J, Nachemson A: Correlation between lactate levels and pH ofpatients with lumbar rizopathies, Experientia, 24, 1195-6, 1968.Nachemson A: Intradiscal measurements of pH in patients with lumbarrhizopathies. Acta Orthop Scand, 40, 23-43, 1969. Keshari K R, Lotz J C,Link T M, Hu S, Majumdar S, Kurhanewicz J: Lactic acid and proteoglycansas metabolic markers for discogenic back pain, Spine, Vol.33(3):312-317, 2008].

As we age, calcified layers 108 form and accumulate at the endplates105, blocking capillaries 107 and further limiting the depth ofdiffusion of nutrients/oxygen/pH buffer 131 into the disc 100, as shownin FIG. 6. Mid layers of the disc 100 suffer chronic and severestarvation and anaerobic conditions. Disc cells can survive withoutoxygen, but die without sugars. Nucleus 128 contains glycosaminoglycanswith covalently bonded sugars, essential for retaining water in the disc100. Degradation of glycosaminoglycans to release sugars for consumptionallows disc cells to survive, but initiates compositional and structuralchange, creating voids 184 and loosely packed nucleus matrix in adegenerated disc 100, as shown in FIG. 7, [Urban J P, Smith S, FairbankJ C T: Nutrition of the Intervertebral Disc, Spine, 29 (23), 2700-2709,2004. Benneker L M, Heini P F, Alini M, Anderson S E, Ito K: Vertebralendplate marrow contact channel occlusions & intervertebral discdegeneration, Spine V30, 167-173, 2005. Holm S, Maroudas A, Urban J P,Selstam G, Nachemson A: Nutrition of the intervertebral disc: solutetransport and metabolism, Connect Tissue Res., 8(2): 101-119, 1981].

Composition Change of the Intervertebral Discs (approximation)

Normal Painful % Change from Discs Discs Normal Discs Glycosamino- 27.4± 2.4% 14.1 ± 1.1% −48.5% glycans Collagen 22.6 ± 1.9% 34.8 ± 1.4%  +54% Water content 81.1 ± 0.9% 74.5 ± 1%    −8.1% Acidity pH 7.14 pH6.65-5.70 [H⁺]: +208% [H⁺]: [H⁺]: to +2.661% 7.20 × 10⁻⁸ 2.23 × 10⁻⁷ to2.00 × 10⁻⁶(Reference: Kitano T, Zerwekh J, Usui Y, Edwards M, Flicker P, Mooney V:Biochemical changes associated with the symptomatic human intervertebraldisk, Clinical Orthopaedics and Related Research, 293, 372-377, 1993.Scott J E, Bosworth T R, Cribb A M, Taylor J R: The chemical morphologyof age-related changes in human intervertebral disc glycosaminoglycansfrom cervical, thoracic and lumbar nucleus pulposus and annulusfibrosus. J. Anat., 184, 73-82, 1994. Diamant B, Karlsson J, NachemsonA: Correlation between lactate levels and pH of patients with lumbarrizopathies, Experientia, 24, 1195-1196, 1968. Nachemson A: Intradiscalmeasurements of pH in patients with lumbar rhizopathies, Acta OrthopScand, 40, 23-43, 1969.)

When glycosaminoglycans diminish, water content and swelling pressure inthe nucleus pulposus 128 decrease. The nucleus 128 with reduced swellingpressure can no longer distribute forces evenly against thecircumference of the inner annulus 378 to keep the annulus bulgingoutward. As a result, the inner annulus 378 sags inward while the outerannulus 378 bulges outward, creating annular delamination 114 andweakened annular layers 378, possibly initiating fissure 121 formationdepicted in FIGS. 5-6. Holes or vacuoles 184 can be found duringdissection of cadaveric discs 100, as shown in FIG. 7. Nucleus pulposi128 of degenerated discs 100 are usually desiccated, with reducedswelling pressure and decreased capability to sustain compressive loads.The compressive load is thus transferred to the facet joints 129,pressing the inferior articular process 143 against the superiorarticular process 142 of the facet joint 129, causing strain, wearand/or pain as shown in FIG. 8 (Dunlop R B, Adams M A, Hutton W C: Discspace narrowing and the lumbar facet joints, Journal of Bone and JointSurgery—British Volume, Vol. 66-B, Issue 5, 706-710, 1984).

A disc 100 with reduced swelling pressure is similar to a flat tire withflexible or flabby side walls. The vertebral body 159 above the soft orflabby disc 100 easily shifts or sways, as shown in FIG. 9. This iscommonly called segmental or spinal instability. As shown in FIG. 10,the frequent or excessive movement of the vertebral body 159 strains thefacet joints 129. Patients with spinal instability often use theirmuscles to guard or support their spines to ease facet pain. As aresult, muscle tension and aches arise, but are successfully treatedwith muscle relaxants. Spinal motions, including compression, torsion,extension, flexion and lateral bending, were measured before and aftersaline injection into cadaveric discs. Intradiscal saline injectionsinto slow leaking cadaveric discs reduced all spinal motions (AnderssonG B J, Schultz A B: Effects of fluid on mechanical properties ofintervertebral discs, J. Biomechanics, Vol. 12, 453-458, 1979).

Discography is a common diagnostic technique for identifying orconfirming a painful disc 100 before surgical intervention. A spinalneedle 102 is guided by a fluoroscope toward the Kambin's Triangle 504in FIGS. 8 and 11, a posterior-lateral area through which spinal needle102 can access a lumbar disc 100 safely. The anterior-posterior view inFIG. 12 guides the needle 102 between endplates 105, but does not showthe ventral-dorsal location of the needle 102 tip. Before passing thepedicle 278 midway, a lateral fluoroscopic view depicted in FIG. 13 mustbe taken to ensure the needle 102 is not too dorsal, entering into theepidural space 119. FIG. 13 depicts the lateral fluoroscopic view,showing the needle 101 tip is ventral to the epidural space 119 and cansafely enter into the mid layer of the disc 100.

In literature, sizable disc 100 puncturing or laceration acceleratesdisc degeneration. In non-painful discs 100, a small spinal needle 460within the spinal needle 102 is used to puncture the disc 100 as shownin FIG. 14. FIG. 15 shows intradiscal injection of X-ray contrast 163,flushing out lactic acid 162 in the disc 100 through fissures 121 toburn the sensory nerve 118, instantaneously causing excruciating painand confirming specific painful disc 100. For normal or non-painfuldiscs, discography is nearly painless. The spinal needle 102 is notshown in FIG. 15. The spinal needle 102 in FIGS. 11-16 allows joining ofdiagnostic discography with therapeutic intervention to relieve backpain during the same visit to save time and reduce pain.

Urinary incontinence is common among women after multiple pregnancies.Weight of the fetus partially rests on the bladder, flattening andwidening the bladder neck and urethral lumen. The sphincteric action ofthe urethral smooth muscle cannot contract far enough to close thewidened lumen for coaptation of urethral mucosa, resulting in urinaryincontinence.

SUMMARY OF INVENTION

A distal portion of a filament is extended beyond the distal end of aneedle with a gripper. A flexible one-way filament retainer with asnagging point is positioned adjacent to the extended filament. Theneedle with the extended filament and the one-way filament retainer areinserted into a cannula. During partial withdrawal of the needle, thesnagging point of the one-way filament retainer hooks or retains thedistal portion of the filament, depositing a section of the filamentbetween the snagging point of the one-way filament retainer and theneedle. When the needle is re-advanced, the needle pushes open theflexible one-way filament retainer, and the section of the filament isexpelled or deposited in tissue. The needle is then rotated; the gripperengages and spirals the expelled filament to burrow into tissue. Theneedle can be further advanced to push and pack the spiral of filamentdeep into the tissue. The process of needle partial withdrawal,re-advancement, rotation and pushing is repeated to pack and fill thetissue with interconnecting spirals of filament. Spirals of filamentrepair intervertebral discs to relieve back pain, or bulk sphincters totreat urinary or fecal incontinence.

The filament has a shape memory property to facilitate packing orspiraling in tissue.

REFERENCE NUMBERS

-   100 Intervertebral disc-   100A L5-S1 disc-   100B L4-5 disc-   100C L3-4 disc-   101 Needle-   102 Spinal needle-   103 Guide wire or tube-   104 Strand in filament-   105 Endplate-   106A Superior diffusion zone-   106B Inferior diffusion zone-   107 Capillaries-   108 Calcified layers-   109 Vascular buds in endplates-   110 Window of cannula-   111 Filament gripper of filament needle-   112 Extension bar-   113 Indentation between snagging points-   114 Annular delamination-   115 Epiphysis-   116 Lumen of dilator-   118 Sensory nerve-   119 Epidural space-   120 Indentation between grippers-   121 Fissure-   123 Spinal cord-   124 Pores of sponge filament-   126 Filament, shunt or disc shunt-   126A U-section or distal portion of filament-   126B Second proximal portion of filament-   126C First proximal portion of filament-   127 Cover or wrapper of filament-   128 Nucleus pulposus-   129 Facet joint-   130 Filament needle handle-   131 Nutrients, oxygen and pH buffering-   132 Cannula handle-   133 Transverse process-   134 Spinous process-   135 Lamina-   140 Ilium or iliac crest-   142 Superior articular process-   143 Inferior articular process-   152 Bobbin-   159 Vertebral body-   160 Biosynthetic product or molecule-   162 Lactic acid-   163 Contrast agent-   184 Hole or void in tissue-   193 Muscle-   194 Spinal nerve root-   195 Posterior longitudinal ligament-   220 Dilator-   230 Cannula-   231 Snagging point, distal edge or rim of cannula-   268 Lumen of cannula-   269 Lumen of filament needle-   276 Syringe-   277 Cell-   278 Pedicle-   378 Annulus or annular layer-   460 Thin spinal needle-   462 Anchor or toggle-   463 Knot-   492 Funnel into lumen of cannula-   493 Marker on filament needle-   494 Flexible holder of the latch-   495 Latch-   496 Slope or slanted surface of latch-   497 Holder of bobbin-   498 Distal protrusion of cannula handle-   499 Proximal protrusion of cannula handle-   500 Distal protrusion of filament needle handle-   501 Proximal protrusion of filament needle handle-   502 Friction ridges of needle handle-   504 Kambin's Triangle (safe entry into disc)-   505 Skin-   516 Urethra-   517 Urethral lumen-   518 Bladder-   519 Bladder neck-   520 Vagina-   521 Pubis-   522 Uterus-   523 Rectum-   524 Posterior wall of urethra-   525 Forceps-   526 Filament advancer-   527 Stem of filament advancer-   528 Barbs or thread of filament advancer-   529 Cone head of dilator-   530 Removable luer lock or dilator handle-   531 Luer lock for syringe-   532 Urethral smooth muscle-   533 Urethral lumen mucosa-   534 One-way filament retainer

DESCRIPTION OF THE DRAWINGS

FIG. 1 shows capillaries 107 in vertebral bodies 159 providing oxygen,nutrients and pH buffer for the avascular intervertebral disc 100through diffusion.

FIG. 2 shows a longitudinal view of a healthy spinal segment withnutrients 131 supplied by capillaries 107 at the vertebral bodies 159and endplates 105 to feed the cells within the disc 100.

FIG. 3 shows a graph of distance into disc from endplate versus oxygenconcentration.

FIG. 4 shows anaerobic production of lactic acid 162 in the mid layer ofthe disc 100, leaking and burning sensory nerve 118 and spinal nerve194.

FIG. 5 shows leakage of lactic acid 162, burning or irritating thespinal nerve 194.

FIG. 6 shows calcified layers 108 at the endplates 105, blockingdiffusion of nutrient, oxygen and pH buffer 131 from capillaries 107,forming and leaking lactic acid 162 to nerve 118.

FIG. 7 shows vacuoles 184 in the disc 100 from degradation ofproteoglycans to release sugars for maintaining survival of disc cells.

FIG. 8 shows load transfer from the flattened disc 100 to facet joint129 causing pain.

FIG. 9 depicts swaying of a vertebral body 159 above a disc 100 withlow-swelling pressure.

FIG. 10 depicts spinal instability from the low-pressure disc 100,straining and wearing down the facet joints 129.

FIG. 11 shows insertion of a spinal needle 102 toward the surface of thedegenerated disc 100 to prepare for diagnostic discography.

FIG. 12 shows a fluoroscopic anterior-posterior view of the needle 102,about half way past pedicles 278, entering into the disc 100.

FIG. 13 shows a fluoroscopic lateral view of the needle 102 enteringinto the disc 100 space, but not into the epidural space 119.

FIG. 14 shows a small spinal needle 460 housed within the spinal needle102, puncturing into the nucleus pulposus 128 of the degenerated disc100.

FIG. 15 depicts pain diagnostic discography by flushing lactic acid 162from disc 100 to sensory nerve 118 with contrast agent 163 to provokeand confirm the excruciating pain.

FIG. 16 shows sliding of spinal needle 102 over small spinal needle 460into nucleus 128.

FIG. 17 shows replacing the small spinal needle 460 with a guide wire103.

FIG. 18 shows replacing the spinal needle 102 with a cone head 529dilator 220.

FIG. 19 shows snagging points 231 at the distal end of a cannula 230.

FIG. 20 shows insertion of the cannula 230 sliding over the dilator 220.

FIG. 21 shows a filament needle 101 with at least one filament gripper111.

FIG. 22 shows a U-shaped filament 126 with the U-portion or distalportion 126A extended from the filament needle 101.

FIG. 23 shows insertion of the filament needle 101 with filament 126into the cannula 230.

FIG. 24 shows the dilator 220 in FIG. 20 is replaced by the cannula 230and needle 101.

FIG. 25 shows the snagging point 231 of the cannula 230 snags thefilament strand 126B during partial withdrawal of the needle 101 todeposit a section of filament 126B, 126C in cannula 230 between distalends of cannula 230 and needle 101.

FIG. 26 shows handle 132 of cannula, handle 130 of filament needle and aspool of filament 126 on a bobbin 152 for feeding into the lumen 269during withdrawal of the needle 101.

FIG. 27 shows re-advancement of the filament needle 101 from FIG. 25,pushing the deposited filament 126B, 126C out of the cannula 230.

FIG. 28 shows filament 126 in nucleus 128 by re-advancing the needle101.

FIG. 29 shows gripping of the filament 126 by the gripper 111 of therotating needle 101.

FIG. 30 shows the needle 101 driving the filament 126 to spiral andburrow into tissue, void 184 or fissure 121.

FIG. 31 shows pushing of the needle 101 to pack and burrow the spiraledfilament 126 into tissue, void 184 or fissure 121.

FIG. 32 shows snagging of the filament 126 by the snagging point 231during withdrawal of the filament needle 101 to deposit additionalfilament 126B, 126C between distal ends of cannula 230 and needle 101.

FIG. 33 shows another re-advancement of the filament needle 101, pushingthe additional deposited filament 126B, 126C out of the cannula 230 intotissue.

FIG. 34 shows the needle 101 driving the filament 126 to form anotherspiral, burrowing into tissue with previously spiraled filament 126.

FIG. 35 shows repeated steps of withdrawal, re-advancement, rotation andpushing of filament needle 101 to form multiple spiraled filaments 126to bulk, fill or fortify tissue.

FIG. 36 shows withdrawal of the cannula 230 and needle 101 after packingthe nucleus 128 of degenerated disc 100 with spirals of filaments 126.

FIG. 37 shows cutting of the filament 126 near the skin 505.

FIG. 38 shows tucking of the filament 126 beneath skin 505 with along-thin forceps 525.

FIG. 39 shows fluid flowing through the filament 126 from low osmoticpressure in muscle 193 to high osmotic pressure in desiccated disc 100.

FIG. 40 shows a longitudinal view of a disc 100 filled with spiraledfilament 126, wicking fluid from muscle 193, superior 106A and inferior106B diffusion zones into mid layer of disc 100.

FIG. 41 shows thickening of the filament-packed disc 100 to reduce facetloading and pain by lifting the inferior articular process 143 of thefacet joint 129.

FIG. 42 shows production of biosynthetic molecules 160 or disc matrix bycells 277 receiving nutrients, oxygen and pH buffer 131 transportedthrough the filament 126.

FIG. 43 shows intradiscal injection of nutrients, oxygen and pH buffer131 and/or cells 277 to facilitate back pain relief and/or disc 100regeneration.

FIG. 44 shows shielding of L5-S1 disc 100A and L4-5 disc 100B by theiliac crest 140, blocking entry of the straight spinal needle 102 ofFIGS. 11 and 14.

FIG. 45 shows iliac crest blocking of the lower lumbar disc 100,preventing entry of spinal needle 102 into the nucleus of the disc 100.

FIG. 46 shows an elastically curved cannula 230 directing a flexiblefilament needle 101 into the center of the disc 100.

FIG. 47 shows normal position of a bladder neck 519 of a woman withurinary control.

FIG. 48 shows funneling or widening of a bladder neck 519 leading tourinary incontinence.

FIG. 49 shows a small spinal needle 460 within a cone-headed 529 dilator220 fastened by a removable luer lock 530.

FIG. 50 shows insertion of cannula 230 and needle 101 to implant aspiraled filament 126 in smooth muscle 532 of the bladder neck 519 undercystoscopic or ultrasound guidance.

FIG. 51 shows a cross-sectional view of a widened urethral lumen 517 andinitial spiral of the filament 126 within the smooth muscle 532 of theurethra 516.

FIG. 52 shows narrowing of the urethral lumen 517 by bulking theurethral smooth muscle 532 with spirals of filament 126 to allowcoaptation of urethral mucosa 533.

FIG. 53 shows two bulking locations of spiraled filaments 126 to closethe urethral lumen 533 and relieve urinary stress incontinence.

FIG. 54 shows bulking of the urethral smooth muscle 532 with spiraledfilament 126, narrowing the urethral lumen 517 at the bladder neck 519to regain sphincteric control.

FIG. 55 shows a knot 463 to prevent retraction of the distal end of thefilament 126A in the needle 101, and to facilitate filament 126 snaggingby the snagging points 231 of cannula 230.

FIG. 56 shows the filament 126C in the needle 101, filament 126B outsidethe needle 101; and the filament 126A is the distal portion betweenfilament 126C and filament 126B.

FIG. 57 shows a linear or single stranded filament 126 tied with a knot463 extending from the needle 101.

FIG. 58 shows an anchor, knob or toggle 462 on a linear filament 126extending from the needle 101 to facilitate filament 126 snagging by thecannula 230.

FIG. 59 shows a cross bar 111 as a filament gripper 111.

FIG. 60 shows the filament 126 looping over the cross bar 111 forfilament 126 spiraling.

FIG. 61 shows a cross plane 111 as a filament gripper 111, dividing thecylindrical lumen 269 into semi-cylinders 269 for housing the filamentstrand 126C and filament strand 126B.

FIG. 62 shows an extended cross bar 111 as a filament gripper 111connecting to extension bars 112. The extended cross bar 111 can also bean extended cross plane within the lumen 269.

FIG. 63 shows the filament 126 looping over the extended cross bar 111or extended cross plane 111 for spiraling and pushing of the filament126.

FIG. 64 shows cross stubs 111 as a filament gripper 111 for spiralingand pushing of the filament 126.

FIG. 65 shows longitudinal cross stubs 111 along the lumen 269 of theneedle 101 for spiraling and pushing of the filament 126.

FIG. 66 shows a filament advancer 526 with resiliently collapsible barbs528, moving in cyclical distal-proximal motion to advance or propel thefilament 126 out of the needle 101.

FIG. 67 shows open and closed positions of the resiliently collapsiblebarb 528.

FIG. 68 shows an axial or vertical view of the filament advancer 526with resiliently collapsible barbs 528 approximately 120 degrees apart.

FIG. 69 shows an axial or vertical view of the filament advancer 526with resiliently collapsible barbs 528 approximately 90 degrees apart.

FIG. 70 shows a rotational auger 526 as a filament advancer 526 toconvey or propel the filament 126 out the needle 101.

FIG. 70A shows a cross section of a needle 101 with a lumen 269configuration to accommodate the filament advancer 526 and filament 126.

FIG. 71 shows a cannula 230 with multiple snagging points 231.

FIG. 72 shows a cannula 230 with a window 110 open to a snagging point231.

FIG. 73 shows snagging points 231 of a cannula 230 with inward bendingor curvatures.

FIG. 74 shows curvatures of snagging points 231 of another cannula 230.

FIG. 75 shows inward bending or curving walls or gates 231 as snaggingpoints 231 at the distal end of the cannula 230.

FIG. 76 shows a cross-sectional view of the inward bending gates 231 ofthe cannula 230.

FIG. 77 shows braided strands 104 forming the filament 126.

FIG. 78 shows woven strands 104 forming the filament 126.

FIG. 79 shows knitted strands 104 forming the filament 126.

FIG. 80 depicts a slanted cut of the filament 126, showing the slantedorientations of strands 104 relative to length-wise of the filament 126.

FIG. 81 shows a cross-section of the filament 126 made with parallelstrands 104 wrapped, encircled, covered or enveloped by a sheath orcover 127.

FIG. 82 shows a cross-section of the filament 126 made with paralleltubes 104 wrapped, encircled, covered or enveloped by a sheath or cover127.

FIG. 83 shows a cross-section of the filament 126 made with sponge orfoam with pores 124.

FIG. 84 shows a cross-section of a solid filament 126, similar to amono-filament suture.

FIG. 85 shows a preformed helical filament 126 in a helical position tofacilitate spiral formation in tissue by the predetermined helicalposition of the preformed helical filament 126.

FIG. 86 shows a preformed zigzag filament 126 in a zigzag or bentposition to facilitate engagement with the snagging point 231 andpacking in tissue.

FIG. 87 shows an oval or elongated cross-section of a needle 101 forgripping a double-stranded filament 126 during needle 101 rotation.

FIG. 88 shows a one-way filament retainer 534 with snagging points 231adjacent to a needle 101.

FIG. 89 shows a one-way filament retainer 534 engaging a filament 126extended from a needle 101.

FIG. 90 shows increase in disc 100 height by bulking and/or hydration ofthe spiraled filament 126 as the internal disc shunt 126.

FIG. 91 shows compression of the disc 100, squeezing or flattening thespiraled filament 126 to discharge nutrient, oxygen and pH buffer 131from the spiraled filament 126 to the disc 100 matrix.

FIG. 92 shows relaxation of the disc 100, allowing expansion of spiraledfilament 126 to draw nutrient, oxygen and pH buffer 131 from shallowendplate 105 diffusion into the spiraled filament 126.

DETAILED DESCRIPTION OF THE EMBODIMENTS

After confirming discogenic pain with discography, the needle 102 isadvanced into the painful disc 100 over the small spinal needle 460, inFIG. 16. The small spinal needle 460 is replaced with a blunt guide wire103 in the spinal needle 102 into the disc 100, in FIG. 17. The proximalend of the guide wire 103 is held stationary during withdrawal of thespinal needle 102 from the patient. The proximal end of the guide wire103 is also held stationary to slide a dilator 220 with a blunt conehead 529 over the guide wire 103 into the disc 100 or tissue, as shownin FIG. 18. A cannula 230 has at least one snagging point 231 andlongitudinal lumen 268, as shown in FIG. 19. The snagging point 231 canalso be a sharp edge 231 with filament gripping or catching capability.The cannula 230 can have a window 110 opened to the lumen 268 and distalopening. While the proximal end of the dilator 220 is held stationary,the cannula 230 is advanced, sliding over the dilator 220 into the disc100, as shown in FIG. 20. The guide wire 103 and dilator 220 areremoved. A filament needle 101 contains at least one gripper 111 and alongitudinal lumen or opening 269 as shown in FIG. 21. Distal end 126Aof a filament 126 is extended from the needle lumen 269 and thefollowing section of the filament 126 is in a straightened position inthe needle 101, as shown in FIG. 22. The distal end 126A of the filament126 can be U-shaped. The filament needle 101 with the filament 126 isinserted into the lumen 268 of the cannula 230 into the disc 100, asshown in FIGS. 23-24. A funnel 492 in the proximal end of cannula handle132 in FIG. 26 is used to facilitate insertion of the filament needle101 of FIG. 22 into the proximal opening of cannula 230.

During partial withdrawal of the filament needle 101 into the cannulalumen 268, the distal portion 126A or extended portion of the filament126 is snagged, caught, hooked, retained, trapped, held or grabbed bythe snagging point 231 in FIG. 25. As a result, the distal portion 126Aor extended portion of the filament 126 remains outside in contact withsurrounding tissue in front of the distal end of the cannula 230; and asection of filament 126B, 126C is in the straightened position,partially deposited in the lumen 268 of cannula 230 between the distalends of the cannula 230 and needle 101, as shown in FIG. 25. A bobbin152 can hold a spool of preformed helical filament 126 in a helicalposition, as shown in FIG. 85. The bobbin is fastened at the proximalend of a needle handle 130, as shown in FIG. 26. During snagging orholding of the distal portion 126A of the filament 126 and partialwithdrawal of the needle 101, additional preformed helical filament 126from the bobbin 152 feeds into the lumen 269 of the needle 101,transforming from the helical position in FIG. 85 to the straightenedposition in the lumen 269. The needle 101 is re-advanced from FIG. 25,pushing or expelling the deposited filament 126B, 126C in front of theneedle 101 out the cannula 230 into tissue, as shown in FIGS. 27-28 toresume the helical position. Excessive withdrawal of the filament needle101 will deposit a long filament 126B, 126C in front of the filamentgripper 111 of the needle 101 within the cannula 230. The long filament126B, 126C within the cannula 230 can jam the re-advancing needle 101. Alatch 495 in FIG. 26 on a flexible spring or nitinol wire 494 extendsfrom a cannula handle 132 to limit and prevent excessive length ordistance of partial withdrawal of the filament needle 101 by stoppingthe proximal protruded end 501 of the needle handle 130. Hence, lengthof filament 126B, 126C deposited within the cannula 230 from partialwithdrawal of needle 101 is short enough to be pushed or expelled outthe cannula 230 by re-advancement of the filament needle 101, as shownin FIGS. 27 and 28. The deposited filament 126B, 126C may also exitthrough the window 110 of the cannula 230 in FIGS. 19 and 27 to avoidjamming during re-advancement of the needle 101. During insertion of thefilament needle 101 in FIG. 22 through the funnel 492 leading into thelumen 268 of the cannula 230, the needle handle 130 slides over theslope 496 of the latch 495 for filament 126 spiraling. FIG. 26 shows amarker 493 on the needle 101. Distal ends of both filament needle 101and cannula 230 are even, as shown in FIG. 23 or 27, when the marker 493lines up at the opening of the funnel 492. When the marker 493 entersinto the funnel 492, the grippers 111 of the needle 101 are extendedoutside the cannula 230 to push and pack the filament 126 into tissue.

Major blood vessels, abdominal aorta, inferior vena cava and commoniliac arteries, are anterior to the lumbar discs. Distal ends of thedevices must remain within the discs 100, confirmable by fluoroscope(X-ray) or markers on the devices to minimize intermittent X-rayexposure to patients and physicians. Markers on proximal ends of theguide wire 103 and dilator 220 help physician to identify deviceorientation. The following table shows lengths and markers on sequentialdevices to guide implantation of spiraled filament 126 into disc 100 torelieve back pain. Markers in the table are measured from the distal endof the device. For safety of the patient, length of a guiding device ispreferred to be longer than the subsequent device, so that the proximalend of the guiding device can be held stationary during insertion of thesubsequent device into patient.

Length, Marker 1, Marker 2, Device OD, mm ID, mm mm mm mm Spinal 1.270.84 172 needle 102 Small spinal 0.51 0.25 226 needle 460 Guide 0.81 492172 338 wire 103 Dilator 220 1.83 1.00 338 185 Cannula 230 2.41 1.97 185Filament 1.83 1.52 230 185 needle 101 Filament 126 0.67-0.77 900 doublestrandsDistal ends of spinal needle 102 and guide wire or tube 103 are even,when Marker 1 of the guide wire 103 is at the proximal end of the spinalneedle 102, as shown in FIG. 17. Distal ends of the dilator 220 andguide wire 103 are even, when Marker 2 of the guide wire 103 is at theproximal end of the dilator 220, as shown in FIG. 18. Distal ends ofcannula 230 and dilator 220 are even, when Marker 1 of the dilator 220is at the proximal end of cannula 230, as shown in FIG. 20. Distal endsof the cannula 230 and filament needle 101 are even, when Marker 1 ofthe needle 101 is at the proximal end of the cannula 230, as shown inFIG. 24.

Annulus 378 of the disc 100 is made mainly with layers of collagen.Layers of collagen form a net-like matrix. Spinal needles 102 or 460with single sharp tips have no problem puncturing through the net-likecollagen matrix of the annulus 378. On the other hand, the cannula 230and filament needle 101 have multiple sharp points 231, 111 at thedistal ends, as forks. The cannula 230 contains indentations 113 betweensnagging points 231 in FIG. 19; and filament needle 101 containsindentations 120 between grippers 111 in FIGS. 21-22. The indentations113, 120 are trapped by the net-like collagen matrix with no annularpenetration capability to prevent possibility of injuring blood vesselsanterior to the discs 100. The guide wire or tube 103 and dilator 220are blunt and have little capability of penetrating annulus 378 toensure safety of the patient.

During pushing and rotation of the filament needle 101, at least one ofthe grippers 111 grabs and spins the extended filament 126B, 126Cburrowing and spiraling into nucleus 128, fissure 121, void 184 or softtissue, as shown in FIG. 29. Spiraling of the extended filament 126 ismade possible by the twisting gripper 111 and friction between theextended filament 126 and tissue. A knot-like spiraled filament 126 isformed due to rotation of the filament needle 101, as shown in FIG. 30.The filament needle 101 can also advance or extend beyond the distal endof the cannula 230 to push, pack, fill, load, cram or stuff the expelledfilament 126, burrowing into nucleus 128, void 184, fissure 121 ortissue, as shown in FIG. 31. The filament needle 101 is partiallywithdrawn again; the extended filament 126 is caught again by thesnagging point 231 of the cannula 230, as shown in FIG. 32. In fact, theinitial spiraled filament 126 also acts as an anchor outside the distalend of the cannula 230; partial withdrawal of the needle 101 deposits orloads additional filament 126B, 126C within the cannula 230 betweendistal ends of cannula 230 and needle 101. The filament needle 101 isre-advanced, pushing or expelling the additional filament 126 out of thecannula 230 into tissue 31, as shown in FIG. 33. Rotations of the needle101 form another spiraled filament 126, linking to the previouslyspiraled filament 126, as shown in FIG. 34. Same direction of needle 101rotations is preferred. Rotation and pushing of the needle 101 help thespiraled filament 126 to seek, burrow and fill void 184, gap, fissure121, vacancy, weak spot, opening, cavity or soft spot. The steps ofneedle 101 withdrawal, re-advancement, rotation and pushing, arerepeated to build, fill, bulk, pack, fortify, load or solidify thetissue with multiple inter-connecting spirals of filament 126, as shownin FIGS. 35-36. Multiple spirals or coils of filament 126 are formed,packed or inserted individually to be shape conforming, malleable and/orresilient in voids 184, yet inter-connected to prevent or minimizemigration from tissue. Rotation and pushing of the needle 101 drive thespirals of filament 126 from the lumen 269 of the needle 101 to seek,fill and pack the distal, lateral and/or proximal space in tissue. Thespirals of filament 126 are remained and probably formed in multipleaxes. Tightness of the spiraled filament 126 is determined by number ofrotations and intensity of pushing of the needle 101. The spiralfilament 126 can be as tight as a suture knot. Fewer rotations and/orgentle pushing of the needle 101 make soft spirals of filament 126.Number of rotations and pushing intensity of the needle 101 can bealternate to allow variations in firmness or density of filament spirals126 within repaired tissue. It is possible to sequential withdraw thecannula 230 from tissue to provide additional distal space for packingadditional spirals of filament 126.

Needle handle 130 and cannula handle 132 are dumbbell shape. The needlehandle 130 has a protruded proximal end 501 and a protruded distal end500 to facilitate withdrawal and advancement of the needle 101, as shownin FIG. 26. The needle handle 130 also contains gripping or frictionridges 502 to facilitate rotation of the needle 101. The cannula handle132 has a protruded proximal end 499 and a protruded distal end 498 tofacilitate withdrawal and advancement of the cannula 230. When thetissue is full with spirals of filament 126, advancement of the needle101 becomes difficult. The cannula 230 can also be slightly andsequentially withdrawn from tissue, to pack or accumulate additionalspirals of filament 126 distal to the cannula 230. A metering device canbe attached to the spool of filament 126 on the bobbin 152 to monitorlength of filament 126 dispensed into patient. When the tissue is packedwith spirals of filament 126, the filament needle 101 and cannula 230are withdrawn from tissue. In the event of disc 100 repair, the extendedfilament 126 is cut above the skin 505, as shown in FIG. 37. Theproximal portions of filament 126B, 126C are tucked beneath the skin 505with a long and thin forceps 525, as shown in FIG. 38. The amount ofimplanted filament 126 is selectable, controllable, limitable orregulateable by the physician.

In summary, the cannula 230 and filament needle 101 work together tospiral the filament 126 or shunt 126 bulking the tissue. The stationarycannula 230 with snagging points 231 prevents the extended filament 126Afrom retrieving or retracting into the lumen 269 of the filament needle101. Additional filament 126 is advanced by eitherwithdrawal/re-advancement of the needle 101 or by a filament advancer526 within the needle 101. Rotation of the needle 101 with grippers 111holds and spirals the filament 126 burrowing into voids 184 and fissure121. The filament spiral 126 is individually formed by spatial allowanceof the tissue, and not spiraling over a spindle, axle, axis or needle.Filament 126 spiraling driven by the rotating needle 101 is spaceseeking, filling, fitting or conforming to fortify, bulk, fill, cushionor repair the tissue. Pushing of the needle 101 further packs thespiraled filament 126 to bulk the tissue.

PCT/US2011/000007, WO/2011/082390 (Internal and external disc shuntsalleviate back pain, by Jeffrey E. Yeung and Teresa Yeung, filed on 3Jan. 2011) contains a U-shaped shunt 126 partly within and partlyoutside a needle 101, and a sleeve 220 sliding over the needle 101.During rotation of the needle 101, the outside draping shunt 126 spiralsover the needle 101 shaft. The sleeve 220 is then advanced distally tostrip the spiraled shunt 126 off the shaft of the needle 101, pushingthe spiraled shunt 126 into the nucleus of the intervertebral disc 100.The sleeve 220 is retrieved to the proximal position. Another spiral ofshunt 126 is formed by rotation of the needle 101, the sleeve 220 isadvanced again to strip the spiraled shunt 126 off the needle 101 intothe nucleus. The process of needle 101 rotation, sleeve 220 advancementand sleeve 220 retrieval are repeated to form spirals of shunt 126within the disc 100. However, many problems occurred during usages ofthis device in clinical study. Due to friction between disc 100 andsleeve 220, advancement of the sleeve 220 for stripping the spiraledshunt 126 from the needle 101 is very difficult. Significant force isrequired to advance the sleeve 220, which adds significant risks ofpuncturing through the disc 100 and rupturing major blood vesselsanterior to the disc 100. In addition, due to direct contact of thesleeve 220 with the painful disc 100, patient feels extreme pain duringadvancement of the sleeve 220 to dislodge the spiraled shunt 126 on theneedle 110. Significant pain is endured during multiple dislodgements ofshunt spirals 126. Fortunately, the patient experienced pain reliefwithin a week due to efficacy of the disc shunt 126.

Unlike PCT/US2011/000007, WO/2011/082390, the cannula 230 in thisapplication is stationary during implantation of the filament 126 intodisc 100 or tissue. The filament needle 101 slides freely within thecannula 230 without risk to the patient or causing pain. The spiral offilament 126 is driven by the grippers 111 and formed distal to therotating needle 101, capable of burrowing, drilling, packing, wiggling,building, dilating, wedging or shimming into voids 184, fissure 121 ortissue. Unlike PCT/US2011/000007, tissue burrowing of the distal formingfilament spiral 126 in this application is particularly effective, deep,and tight, as shown in FIG. 30, embedding, filling, packing and bulkingthe tissue as shown in FIG. 36. The spiraled filament 126 inPCT/US2011/000007, WO/2011/082390 is already formed on the needle 101shaft, which may not fit into small voids 184 or fissures 121. Inaddition, spiraling of the filament 126 in this application isparticularly unique. Filament 126 spiraling can occur only in tissue,interference or friction surrounding the extended filament 126,different from disc shunt 126 spiraling the over the needle 101, astaught in PCT/US2011/000007, WO/2011/082390.

Fluid flows from low to high osmotic pressure according to the law ofphysics. Osmotic pressure of blood plasma in muscle 193 is approximately250-300 mOsm/liter; intervertebral disc 100 is 300-400 mOsm/liter.Through the difference between osmotic pressures, the connectingfilament 126 draws fluid from muscle 193 to hydrate the desiccatednucleus 128 without a pump, as shown in FIG. 39.

In-vitro study, the filament 126 was implanted into sheep discs 100 (430mOsm/liter) and human cadaver discs 100 (300-400 mOsm/liter) of variousdegenerative levels, Thompson Grade 0-4. The discs 100 with filaments126 were submerged in saline with blue dye (300 mOsm/liter). Dissectionof the discs 100 showed blue saline permeation into the nuclei 128,confirming fluid flows from low to high osmotic pressure.

Another filament 126 was implanted through a muscle into a sheep disc100. The sheep muscle 193 was saturated with iopamidol (contrast agentwith blue dye, 545 mOsm/1). The blue iopamidol did not permeate throughthe filament 126 into the sheep disc 100 (430 mOsm/liter). In fact thedissected disc 100 looked desiccated; fluid within the sheep disc 100was probably drawn into the muscle 193 infused with 545 mOsm/liter blueiopamidol through the filament 126. The experiment was repeated withdiluted blue iopamidol solution (150 mOsm/liter). The diluted iopamidolsolution saturated the muscle 193 and permeated through the filament 126into the sheep disc 100 visible and traceable from muscle 193 to nucleus128 under CT. Dissection confirmed permeation of the diluted blueiopamidol into the nucleus 128 of the sheep disc 100. Again, fluid flowsfrom low to high osmotic pressure through the filament 126.

Sheep discs were implanted with filaments 126 and submerged in porkblood (about 320 mOsm/liter). Dissection of the discs 100 showedpermeation of pork blood through the filament 126 into the nuclei of thesheep discs 100 (430 mOsm/liter).

Gradient of pH is formed in the disc 100 due to shallow diffusion of pHbuffer 131 from the capillaries 107 at the endplates 105. The superior106A and inferior 106B diffusion zones are approximately 0-2 mm from thesuperior or inferior endplates 105. The pH in the superior 106A andinferior 106B diffusion zones is neutral. Acidity increases at the midlayer of the disc 100, where chronic deprivation of oxygen, nutrientsand pH buffer occurs. FIG. 40 shows a longitudinal view of a filament126 filled disc 100 with calcified layers 108 accumulated over theendplate 105. The hydrophilic spiraled filament 126 reaches, locates,resides or contacts at least one of the superior 106A and inferior 106Bdiffusion zones, drawing and transporting nutrients/oxygen/pH buffer 131to neutralize lactic acid 162 and nourish cells in the mid layer of thedisc 100. As a result, lactic acid 162 burn is minimized and back painis relieved. In essence, the spiraled filament 126 bridges, links ortransports fluid between source of oxygen/nutrients/pH buffer 131 andmid layer of the disc 100 to treat the etiology and symptom of backpain. Furthermore, oxygen 131 from the muscle 193, superior 106A andinferior 106B diffusion zones converts anaerobic conditions into aerobicwithin the mid layer of the disc 100 to further reduce production oflactic acid 162 and relieve back pain.

The filament 126 can be further identified as internal filament 126 andexternal filament 126. The filament 126 in the disc 100 can be calledthe disc shunt 126 to form as internal shunt 126 between superiordiffusion zone 106A and inferior diffusion zone 106B. The disc shunt 126extending from disc 100 to body circulation or muscle 193 is calledexternal shunt 126. The disc shunt 126 is a fluid-transferring ordelivery device, inserted into the nucleus 128 of a degenerated disc100. Due to relaxation and compression of the disc 100 from dailyactivities of the patient, spiraled internal shunt 126 in the disc 100facilitates transport of oxygen/nutrients/pH buffer 131 through out thedisc 100. During relaxation, oxygen/nutrients/pH buffer 131 fromdiffusion zones 106A, 106B are absorbed by the internal shunt 126, andoxygen/nutrients/pH buffer 131 in muscle 193 are drawn through theexternal filament 126. During compression, oxygen/nutrients/pH buffer131 in the shunt 126 are expelled to neutralize lactic acid 162 and fedto disc cells in the mid layer of the disc 100. Essentially, bothdiffusion zones 106A, 106B are expanded to cover the mid layer or acidiclayer of the disc 100. Hence, fluid leaking from the fissure 121 is pHneutral or near pH neutral to alleviate back pain, as shown in FIG. 40.Fluid transport or distribution is made possible by soft and pliablespirals of filament 126 as internal disc shunt 126 with hydrophilic andmalleable properties, absorbing and delivering nutrients/oxygen/pHbuffer 131 within the avascular disc 100. Fluid flow through the shunt126 is dynamic and continuous with potential to rebuild disc matrix fordisc regeneration.

Nutrients/oxygen/pH buffers 131 are diffused from the capillaries 107 atthe endplates 105 into the nutrient-poor avascular disc 100, as shown inFIG. 40. Diffusion is concentration related; solutes move from high tolow concentration, from capillaries 107 into diffusion zones 106A, 106B.Withdrawal of nutrients/oxygen/pH buffers 131 by the internal shunt 126leads to additional diffusion of nutrients/oxygen/pH buffers 131 fromcapillaries 107 and vascular buds. The net supply of nutrients/oxygen/pHbuffer solutes 131 into the disc 100 will increase with implantation ofthe internal shunt 126 as shown in FIG. 40. Distribution ofnutrients/oxygen/pH buffer 131 is expanded by the internal shunt 126covering or permeating the full-thickness of the intervertebral disc 100to neutralize lactic acid 162, nourish starving disc cells 277 andrebuild disc matrix to sustain compressive loading of the disc 100.

Depending on severity of the calcified layers 108 covering thecapillaries 107 and vascular buds at the endplates 105, the superior106A and inferior 106B diffusion zones containing nutrients/oxygen/pHbuffer 131 are between 0 and 5 mm from the cartilaginous endplates 105.For degenerated and/or painful discs 100, the superior 106A and inferior106B diffusion zones are likely between 0 and 2 mm from the superior andinferior endplates 105. Hence, the internal disc shunt 126 should reachat least one, but preferably both superior 106A and inferior 106Bdiffusion zones, between 0 and 3 mm from both endplates. Repetitiveformations and deployments of the coiled or spiraled shunt 126 is usedto position, reside, locate, reach or contact at least one diffusionzone 106A or 106B, between 0 and 2 mm from at least one endplate 105 toform the internal disc shunt 126. Distance of the internal shunt 126from the endplate 105 determines availability or quantity ofnutrients/oxygen/pH buffer 131 for supplying the mid layer of the disc100 to alleviate discogenic pain from lactic acid 162 burn.

Due to avascular nature, intervertebral disc 100 is immuno-isolated.In-vivo sheep study, there was no tissue response within the discs 100to nylon filament 126 after 1, 3, 6, 12 and 30 months, using H&Ehistology staining. No fibrotic encapsulation over the nylon filament126 was observed within the discs 100. Similarly, there was nonoticeable inflammatory reaction to the nylon filament 126 in a humanpilot clinical study in 1 week, 3, 6, 12 and 24 months. Internaltransport of nutrients/oxygen/pH buffer 131 from superior 106A and/orinferior 106B diffusion zones continues without hindrance of fibroticencapsulation over the filament 126 within the intervertebral disc 100.

The multiple coils or spirals of filament 126 or shunt 126 provide bulk,shimming, filling, cushion, mass, wedging or fortification within thedisc 100 to elevate, raise, lift, increase or sustain disc 100 height asindicated by arrows in FIGS. 40-41. Spirals of filament 126 bulk up thenucleus 128 to elevate or support disc height for sustaining axialcompression, stiffen the disc 100 for reducing spinal instability,and/or lift the inferior articular process 143 of the facet joint 129 toreduce facet pain, as shown in FIG. 41.

Nutrients/oxygen/pH buffer 131 transported through the filament 126 feedcells 277 to produce biosynthetic molecules, which can beglycosaminoglycans, collagen or disc matrix, as shown in FIG. 42. Cells277 and nutrients/oxygen/pH buffer 131 can be intradiscally injected, inFIG. 43, to expedite disc 100 regeneration and pain relief.

Lower lumbar L5-S1 disc 100A and L4-5 disc 100B are shielded by a pairof iliac crests 140, as shown in FIG. 44. The straight spinal needle 102enters superiorly over the iliac crest 140 at an angle, as shown in FIG.45, difficult or even impossible to deliver the shunt 126 into thenucleus 128 of the disc 100.

FIG. 46 shows an elastically curved cannula 230 leading the filamentneedle 101 into the nucleus 128 of a degenerated disc 100. Theelastically curved cannula 230 is resiliently straightened by slidingover the dilator 220 into the annulus 378 of the disc 100. Then, thedilator 220 is partially withdrawn while holding the cannula stationary.The cannula 230 resumes the curvature and advances into the looselypacked nucleus 128. After confirming distal location of the curvedcannula 230 by fluoroscope, the filament needle 101 in FIG. 22 replacesthe dilator 220 for filament 126 spiraling, similar to FIGS. 25, 27-39.The cannula 230 and needle 101 can be made with nickel titanium alloyfor shaped memory and super elasticity.

In summary, insertion of the spiraled filament 126 into disc 100increases nutrients/oxygen/pH buffer 131 from muscle 193 and diffusionzones 106A and/or 106B to reduce lactic acid 162 burn and feed cells.The spiraled filament 126 also adds bulk and cushion to reduce spinalinstability and facet pain.

The shunt 126 for disc 100 repair is hydrophilic with measurablecharacteristics under ambient temperature and pressure for transportingand retaining fluid to relieve pain and/or regenerate the degenerateddisc 100. After saturation in water, the shunt 126 gains weight between10% and 500% by absorbing water within the matrix of the shunt 126. Ahealthy human disc 100 contains 80% water. The preferred waterabsorbency after water saturation is between 30% and 120%. The shunt 126can have pore sizes between 1 nano-meter and 500 micro-meters, servingas water retaining pockets or water transporting channels. Pores 124 ofthe shunt 126 also function as scaffolding or housing for cell 277attachment and cellular proliferation, as shown in FIG. 42. Watercontact angle on the shunt 126 is between 0 and 60 degrees. Thepreferred water contact angle of the shunt 126 is between 0 and 30degrees. Height of capillary action for drawing saline up the shunt 126is between 0.5 and 120 cm. The preferred height of capillary action ofdrawing saline is between 1 and 60 cm. Height of capillary action fordrawing pork blood up the shunt 126 is between 0.5 and 50 cm. Thepreferred height of capillary action for drawing pork blood up the shunt126 is between 1 cm and 25 cm. Saline siphoning transport rate throughthe shunt 126 is between 0.1 and 10 cc per 8 hours in a humiditychamber. Human lumbar disc 100 loses between about 0.5 and 1.5 cc fluidper day due to compression. The saline siphoning transport rate throughthe shunt 126 is preferred between 0.5 and 5 cc per 8 hours in ahumidity chamber. Pork blood siphoning transport rate through the shunt126 is between 0.1 and 10 cc per 8 hours in a humidity chamber. The porkblood siphoning transport rate through the shunt 126 is preferredbetween 0.5 and 3 cc per 8 hours in a humidity chamber.

The shunt 126 used in the sheep and human clinical studies have thefollowing physical properties under ambient temperature and pressure:(1) weight gain 80% after water saturation, (2) water contact angle zerodegree, (3) height of capillary action 11 cm with pork blood, 40 cm withsaline with blue dye, and (4) rate of siphoning pork blood 1.656+/−0.013cc per 8 hours in a humidity chamber.

Average lactic acid concentration in painful lumbar disc 100 is about14.5 mM, 15 cc or less in volume (Diamant B, Karlsson J, Nachemson A:Correlation between lactate levels and pH of patients with lumbarrizopathies. Experientia, 24, 1195-1196, 1968). An in-vitro study wasconducted to show instant lactic acid neutralization by blood plasma.The spiraled shunt 126 was formed within, and then extracted from afresh portion of beef. Blood plasma absorbed in the spiraled shunt 126instantly neutralized 42% of the 14.5 mM, 15 cc of lactic acid solution,measurable by a pH meter.

Approximately 85% back pain patients show no nerve impingement under MRIor CT. A patient without nerve impingement suffered chronic back painwith visual analog score 8-9 out of 10 (most severe), and leg pain withvisual analog score 8. Five days after implantation of the shunt 126,the visual analog score dropped to 2.5 for her back pain, but the visualanalog score persisted at 8 for leg pain. In the 5.5-month follow-up,the visual analog score dropped to 2.0 for her back pain, and visualanalog score dropped from 8 to zero for leg pain. Quick back pain reliefmay be contributed to instant lactic acid 162 neutralization by bloodplasma of the patient to relieve acid burning of the adjacent sensorynerves 118. Leg pain may be caused by acid scaring of the spinal nerve194 and chemical radiculitis, which takes time to heal and relieve thepain. In human clinical study, the outer diameters of the needle 101 andcannula 230 are only 1.83 and 2.41 mm respectively. The outer diameterof the shunt 126 is 0.55-0.77 mm.

Urinary incontinence is common among women, especially after multiplepregnancies and vaginal deliveries. Major urethral sphincteric action isoperated by smooth muscle 532 at the bladder neck 519. FIG. 47 shows anormal and narrow bladder neck 519 of a woman with urinary control. Thesmooth muscle 532 controls opening and closure of the urethral lumen 517lined with mucosa 533. During pregnancy, the fetus presses against thebladder 518 and the urethra 516 for months. The downward compressionflattens and widens the smooth muscle 532 and urethral lumen 517 of thebladder neck 519, as shown in FIG. 48. A widened lumen 517 at thebladder neck 519 is beyond the range of sphincteric closure of thesmooth muscle 532 for coaptation of mucosa 533 in urethral lumen 517. Asa result, stress urinary incontinence occurs during increased abdominalpressure from coughing, sneezing, laughing or even standing. In surgicalintervention for stress incontinence, the vagina 520 is pulled andfastened to ligaments anteriorly, to support and push forward theposterior wall 524 of the bladder neck 519, narrowing the urethral lumen517 for coaptation of urethral mucosa 533 during sphincteric action.

A needle 460 within a cone-head dilator 220 in FIG. 49 is inserted intourethral smooth muscle 532 of the bladder neck 519 under cystoscopic orultrasound guidance. An echogenic gel can be injected through the needle460 to confirm location of the needle 460 tip within the urethral muscle532. The cone-head dilator 220 slides over the needle 460 into theurethral muscle 532. The needle 460 is withdrawn. Addition echogenic gelcan be injected through the removable luer lock 530 to ensure locationof the dilator 220 tip within the urethral muscle 532. The luer lock 530is removed to prepare for repair. Similar to disc 100 repair, a cannula230 slides over the dilator 220 into the urethral muscle 532. Thedilator 220 is replaced with a filament needle 101 loaded with filament126 within the cannula 230, as shown in FIG. 23. Spiraled filament 126in FIG. 50 is created by withdrawal, advancement, rotation and pushingof the filament needle 101, as shown in FIGS. 25, 27 and 29-35. FIG. 51shows an axial or cross-sectional view of the urethra 516 with a widenedurethral lumen 517 and initial spiraled filament 126 formed within thesmooth muscle 532 of the posterior wall 524 of the urethra 516. FIG. 52shows bulking, enlargement or filling of the urethral smooth muscle 532with spirals of filament 126 at the posterior wall 524 to encroach orextend into the space of urethral lumen 517, resulting in size reductionof the urethral lumen 517 to facilitate coaptation of urethral mucosa533 during sphincteric action of the urethral muscle 532. Multiplelocations of spiraled filaments 126 can be implanted in urethral muscle532 to further narrowing the urethral lumen 517, as shown in FIG. 53.For bulking of urethra 516, no filament 126 should be extended into thelumen 517 to avoid infiltration of bacteria into the smooth urethralmuscle 532. When closure of urethral lumen 517 with bulking of thefilament 126 seems adequate through the cystoscope, the filament 126between the proximal end 501 of needle handle 130 and bobbin 152 in FIG.26 is cut, and spiraling of the filament 126 continues with withdrawal,re-advancement and rotation of the needle 101 to completely spiral theremaining filament 126 in needle 101 into urethral muscle 532. Theamount of implanted filament 126 is selectable, controllable, limitableor regulateable by the physician. The filament 126 can be a nylon,polypropylene or biodegradable mono-filament suture with some stiffnessor shape memory. Coiling or spiraling of the shape memory filament 126expands within tissue to provide elastic bulking or expansion to enhancethe backboard support and sphincteric action of the urethra 516. FIG. 54shows narrowing of the bladder neck 519 by spirals of filament 126cushioning, bulking or supporting tissue between the vagina 520 andurethral lumen 517 to relieve stress urinary incontinence and regainsphincteric control.

Gel-like bulking agent has been injected into fecal sphincteric muscleto treat fecal incontinence, but feces can be substantially firm andlarge to flatten and nullify bulking of the gel-like agent. On the otherhand, the elastic and shape-memory spirals of filament 126 areinter-connected to prevent flattening, migration or dislocation, tomaintain fecal sphincteric bulking and control, similar to urethralbulking in FIGS. 49-54.

The filament 126 can be a suture 126. The suture 126 spiraling devicecan also be used to spiral and pack suture 126 under skin to fillindentations from acne scar or cosmetic defect. The spirals of suture126 at the distal end can also be used as a suture anchor deep withintissue. The proximal end of the suture 126 can be threaded with a tissuerepairing needle for tissue fastening through micro-invasive procedure,such as face lift and other suture repair.

The filament 126 or strands 104 of the filament 126 can expand or swellduring hydration in body fluid. The swelled filament 126 adds size ormass within tissue to enhance bulking or efficacy of the spirals offilament 126. The filament 126 can also be coated with a hydrophilic orswelling agent, such as polyethylene glycol, collagen, hyaluronic acidor other, for expansion.

The dilator 220 in FIG. 49 can be substituted with the cannula 230connecting to a luer lock 531 at the proximal end for injection ofechogenic liquid. After needle 460 puncturing into urethral muscle 532,the cannula 230 is advanced by sliding over the needle 460 into urethralmuscle 532. The needle 460 is withdrawn. Echogenic gel or liquid can beinjected through the cannula 230 to confirm distal location of thecannula 230 in urethral muscle 532. Since the cannula 230 has no tissuepuncturing capability, injection of echogenic gel for locationconfirmation may not be necessary. The filament needle 101 is insertedinto the cannula 230 for spiraling filament 126.

A knot 463 can be tied at the distal portion 126A of the filament 126 toprevent retrieval of the filament 126 into the straightened positionwithin the lumen 269 of the needle 101, as shown in FIG. 55. The knot463 also facilitates catching or hooking by the snagging point 231 ofthe cannula 230, further improved from FIG. 25. The U-strand of thefilament 126 can be divided into distal portion 126A and proximalportions 126B and 126C. A proximal portion 126B of the filament 126 candrape outside, while another proximal portion 126C of the filament 126can be inserted in the needle 101 as shown in FIG. 56. A single strandedfilament 126 can be inserted into the needle 101, as shown in FIG. 57.The single stranded filament 126 can also be snagged by the snaggingpoints 231 of the cannula 230 and rotated into spiraled filament 126. Aknot 463 is tied at the distal portion 126A to prevent retrieval of thesingle stranded filament 126 into the lumen 269 of the needle 101, asshown in FIG. 57. An anchor 462 can be attached at the distal end of thefilament 126, as shown in FIG. 58. The anchor 462 can be made with abiodegradable material or tablet of a pH buffer, nutrients ormedication. The anchor 462 can also be a toggle 462, a protrusion 462 orlatch 462.

The filament gripper 111 can be a cross bar 111 as shown in FIG. 59. Thefilament 126 loops over the cross bar 111, as shown in FIG. 60, forinsertion into the cannula 230. The cross bar 111 can be a longitudinalplane, dividing the cylindrical lumen 269 of the needle 101 into twosemi-cylindrical lumens 269, as shown in FIG. 61. The cross bar 111 orcross plane 111 can tightly pack the spiraled filament 126 into tissue.The cross bar 111 can be extended by two extension bars 112 as shown inFIG. 62. The filament 126 loops over the extended cross bar 111, asshown in FIG. 63. The extended cross bar 111 can also be extended into across plane 111, dividing into two semi-cylindrical lumens 269. Filamentgrippers 111 can be cross stubs 111 as shown in FIG. 64. The cross stubs111 can also be two longitudinal stubs length-wise through the lumen269, as shown in FIG. 65.

Loading filament 126 from the bobbin 152 into proximal lumen 269 of theneedle 101 is driven by holding the distal end 126A of the filament 126and withdrawing the needle 101, as shown in FIGS. 25, 26 and 32. Afilament advancer 526 can be manually used or motorized to advance thefilament 126 without needle 101 withdrawal. The filament advancer 526contains a stem 527 attaching resiliently collapsible barbs 528 pointingdistally, as shown in FIG. 66. The resiliently collapsible barbs 528have a closed and open positions. In the closed position, the distalends of the resiliently collapsible barbs 528 approximate the stem 527,solid lines of FIG. 67. In the open position, the distal ends of theresiliently collapsible barbs 528 depart or move outward from the stem527, in dashed lines of FIG. 67. In operation within tissue, distal endof the filament advancer 526 and the resiliently collapsible barbs 528are concealed and operated within the lumen 269 of the needle 101. Theneedle lumen 269 can be non-circular shape. Cross-section of the lumen269 can contain two connecting circular lumens 269, one for housing thefilament advancer 526 and the other for housing the filament 126,similar configuration as FIG. 70A. The opening between the twoconnecting circular lumens 269 allows the collapsible barbs 528 toextend and engage with the filament 126. During distal movement of thefilament advancer 526, the collapsible barbs 528 are in the openpositions to grip, puncture, insert, hold, grab, attach, engage, hook orlatch on the filament 126, moving the filament 126 distally. Duringproximal movement of the filament advancer 526, the resilientlycollapsible barbs 528 release the engagement with the filament 126 andretract, retrieve or collapse into the closed positions to approximatingthe stem 527. The collapsible barbs 528 are elastic or flexible to gripand release the filament 126 during cyclical distal-proximal movement ofthe stem 527 or filament advancer 526. The collapsible barbs 528 arespaced out along the stem 527. The axial or vertical view of thefilament advancer 526 in FIG. 68 shows orientations of the resilientlycollapsible barb 528 approximately 120 degrees apart. FIG. 69 shows thecollapsible barbs 528 approximately 90 degrees apart. The filament 126can also be advanced by a manually driven or motorized rotational auger526 as filament advancer 526 within the lumen 269 of the needle 101, asshown in FIG. 70. The auger 526 contains a stem 527 and screw-like orhelical thread 528 to engage, convey or propel the filament 126 out theneedle 101. In operation within tissue, distal end of the filamentadvancer 526 and the screw-like thread 528 are concealed and operatedwithin the lumen 269 of the needle 101. The needle lumen 269 can also benon-circular shaped. Cross-section of the lumen 269 can contain twoconnecting circular lumens 269, one for housing the rotational auger 526and the other for housing the filament 126, as shown in FIG. 70A. Theopening between the two connecting circular lumens 269 allows thescrew-like thread 528 to extend and engage with the filament 126. Themotorized speed of the resiliently collapsible barbs 528 and screw-likethread 528 can be controlled by a foot pedal. During high torque, atorque sensor initiates reduction or stopping of the motor. Themotorized filament advancer 526 saves surgical time and allows physicianto concentrate on needle 101 rotation and pushing to pack filament 126for repairing tissue. The resiliently collapsible barbs 528 and thescrew-like thread 528 can be called the filament engager 528 of thefilament advancer 526.

FIG. 71 shows a cannula 230 with multiple snagging points 231 tofacilitate holding on the filament 126. FIG. 72 shows a large window 110for filament 126 to protrude during needle re-advancement to preventjamming. The window 110 is open to a snagging point 231. FIG. 73 showselastically curved or inward bending of snagging points 231 of thecannula 230 to facilitate trapping or hooking of the extended filament126 in FIGS. 22-25, 27-28, 32, 46, 50, 55-58, 60, 63 from the needle101. The cannula 230 with elastically curved snagging points 231 can bemade with nickel-titanium alloy or nitinol. During advancement of thefilament needle 101, the elastically curved snagging points 231resiliently open or straighten to allow passing of the needle 101 andthe extended filament 126. The elastically curved snagging points 231provide inward grip to trap, catch or hook the extended filament 126,similar to the result of FIGS. 25 and 32. Other elastically curvedsnagging points 231 of the cannula 230 are shown in FIG. 74. Thesnagging points 231 can be elastically curved walls or gates 231 at thedistal end of the cannula 230 in FIG. 75 to hook or trap the extendedfilament 126 from the needle 101. FIG. 76 shows a cross-sectional viewof the inward bending or elastically curved gates 231, restricting thedistal lumen 268 of the cannula 230. The elastic snagging point 231 canbe called a spring biased arm 231.

Flexible filament 126 can be made or formed by fabric making techniques,such as braiding or twisting strands 104 as shown in FIG. 77. Fortwisting, minimum number of strands 104 is two. For braiding, minimumnumber of strands 104 is three, as shown in FIG. 77. Braiding orintertwining three or more strands 104 provides excellent flexibility,strength and porosity of the filament 126. The snagging point 231 ofcannula 230 and gripper 111 of needle 101 can catch, snag or engage thefilament 126 well. The flexible filament 126 can also be woven, as shownin FIG. 78. Weaving is interlacing the strands 104 over and under eachother, generally oriented at 90 degree angles. Half of the strands 104from weaving can be oriented length-wise along the linear filament 126,to expedite capillarity or fluid flow from the muscle 193 or diffusionzones 106A, 106B into the degenerated disc 100. The flexible filament126 can be knitted, as shown in FIG. 79. Knitting is a construction madeby interlocking loops of one or more strands 104. A knitted filament 126may have the greatest elastic expansion and compression capability,delivering the most fluid transport or exchange between disc 100 andbody circulation during compression and relaxation of the disc 100. Inaddition, the knitted filament 126 in coils, spirals or reels may havethe highest porosity to enhance fluid absorbency, creating a reservoirof nutrients/oxygen/pH buffer 131 for dispersing into various parts ofthe avascular disc 100, as shown in FIGS. 39-40. Furthermore, the coiledor spiraled filament 126 with knitted strands 104 provides an elasticcushion within the disc 100 to reduce loading and pain in the facetjoints 129. The knitted filament 126 may be an excellent matrix orscaffolding for cell 277 attachment and proliferation. The knittedfilament 126 may also provide highly expandable spirals for bulkingsphincters to regain urinary or fecal control. The filament 126 can bemade with non-woven strands 104. The term non-woven is used in fabricindustry to include all other techniques, such as carded/needle-punched,spunbonded, melt blown or other. Non-woven filament 126 can providelarge surface area as scaffolding for cell 277 growth and proliferation.Combinations of fabric making techniques for the filament 126 can alsobe used with the needle 101 and cannula 230.

Material and/or orientation of the filaments 126 can affect (1) flowrate, (2) tensile strength, (3) annular sealing, (4) porosity, (5) fluidabsorbency, (6) snagging ability, (7) elasticity, (8) selectivity ofsolute transport, (9) scaffold attachment of cells, (10) flexibility,(11) durability, (12) sterilization technique, (13) fibrotic formation,(14) biocompatibility, and/or (15) bulking. A filament 126 is cut at aslanted angle, showing a cross-section of a filament 126; the strands104 are slanted or diagonally oriented to the length-wise filament 126,as shown in FIG. 80. FIG. 81 shows cross-sections of strands 104parallel to the filament 126, covered by a wrapper, sheath or cover 127.The parallel-oriented strands 104 and wrapper 127 can be manufactured byextrusion. The strands 104 can also be micro tubes, as shown in FIG. 82,parallel to the filament 126. A wrapper 127 is used to cover, retain,enclose or house the micro strands 104 to form a filament 126. Anindividual micro tubular strand 104 is capable of having capillaryaction, drawing nutrients/oxygen/pH buffer 131 through the filament 126into the disc 100.

The strands 104 are preferred to be made with biocompatible andhydrophilic material, absorbing, retaining or drawing fluid withnutrients/oxygen/pH buffer solutes 131 from a tissue with low osmolarityto mid layer of the desiccated disc 100 with high osmolarity. Thefilament 126 can be a suture, approved for human implant. Instead offastening tissue, the suture is used as the filament 126, transportingfluid from low to high osmolarity to alleviate back pain.

The filament 126 can be made with a hydrophilic sponge or foam withpores 124, as shown in FIG. 83, to transport and retain fluid in thedisc 100. The pores 124 can be open, connecting to other pores 124. Thepores 124 can also be closed, not connecting to other pores 124 toretain fluid and cells 277. The filament 126 can be solid, pore-less ordense, as shown in cross section in FIG. 84. The solid filament 126 issimilar to a mono-filament suture 126. The mono-filament 126 isrelatively stiff or contains a shape-memory to resist a spiral or coiledconfiguration. The spiraled mono-filament 126 elastically expands withintissue, which is suitable for elastic bulking of sphincters to treaturinary or fecal incontinence.

FIG. 85 shows a preformed helical filament 126 in a helical position.FIG. 86 shows a filament 126 in a zigzag, or bent form. The helical orzigzag position of the filament 126 in FIGS. 85-86 can be transformedinto a straightened position in the needle 101, as shown in FIGS. 23-24.The extended filament 126 in FIGS. 27-28, 33 resumes the helical orzigzag, position to engage the snagging point 231 of cannula. Thepreformed helical filament 126 in FIG. 85 provides a shape to facilitateand maintain spirals of filament 126 within tissue during and afterneedle rotation as shown in FIGS. 29-30, 34-35. In fact, the preformedhelical filament 126 may not require rotation of the needle 101 to formspiraled filament 126 in tissue. The zigzag or bent in FIG. 86facilitates directional shift during spiraling of the filament 126 intissue. The zigzag or bent disperses spirals of filament 126 withintissue. Directional shift of the preformed zigzag filament 126 increasespacking, loading, filling, bulking or fortification in tissue.Otherwise, the spiraled filament 126 would mainly accumulate at oraround the head space, distal to the needle 101.

The shape memory of the filament 126 can be made by temperaturetreatment, block polymers, spinning method, bi-component spinningmethod, weaving method, knitting method, extrusion or other method.

The filament 126 can also be made with an elastic material. Tissueaugmentation or bulking with an elastic spiraled filament 126 providesadditional comfort and increases range of tissue function, especiallyfor bulking mucosal wall of bladder neck to treat urinary incontinence,or bulking fecal sphincter to treat fecal incontinence. The elasticfilament 126 can also be made by a coating of an elastic or swellablematerial, such as collagen, hyaluronate, proteoglycan, polyurethane,silicone or other biocompatible material.

A cross-section of the needle 101 can be oval or elongated to house adouble-stranded filament 126, as shown in FIG. 87. During twisting orrotation of the needle 101, the oval or elongated cross-sectional lumen269 of the needle 101 grips or holds the double-stranded filament 126 inthe straightened position to spiral the extended shape determinedfilament 126 in tissue, without needing the teeth 111 in FIGS. 29-30.The inside diameter of the cannula 230 in FIGS. 29-30 would be increasedto accommodate the oval or elongated cross-section of the needle 101.

FIG. 88 shows a one-way filament retainer 534 with snagging points 231adjacent to a needle 101. The one-way filament retainer 534 is curved,flexible and/or super elastic. The one-way filament retainer 534 is alsothin as a ribbon. The needle 101 with extended filament 126 and theone-way filament retainer 534 are inserted into the cannula 239 intissue, as shown in FIG. 89. During partial withdrawal of the needle101, the filament 126 is caught, hooked, retained, held or engaged bythe snagging point 231 of the one-way filament retainer 534. A sectionof the filament 126 is deposited between the snagging point 231 anddistal end of the needle 101. During re-advancement of the needle 101,the needle 101 pushes open the flexible one-way filament retainer 534and deposits the section of the filament 126 in tissue, similar to FIG.27. The flexible one-way filament retainer 534 prevents retrieval of thefilament 126 from tissue. The flexible one-way filament retainer 534retains the filament 126 for repeating cycle to build spiraled filament126, which includes the steps of partial needle 101 withdrawal,re-advancement of the needle 101, and rotation of the needle 101. Theflexible one-way filament retainer 534 can be withdrawn from the cannula230 after several filament spirals 126, which became larger than theinner diameter of the cannula 230.

FIG. 90 shows increase in disc 100 height by bulking and/or hydration ofthe spiraled filament 126 as the internal disc shunt 126. Increase indisc height relieves load, strain and pain from facet joints, which iscommon among back pain patients. Bulking or hydration of the spiraledfilament 126 within degenerated disc 100 also stabilizes the spinalsegment to reduce pain from instability.

The spiraled filament 126 has volume altering or changing property forfluid discharging and absorption, similar to a biocompatible sponge,fabric or cloth. During compressions of the intervertebral disc 100 indaily activities, the spiraled filament 126 is squeezed or flattened todischarge nutrient, oxygen and pH buffer 131 from the pores and strands104 of spiraled filaments 126 into the disc 100 matrix to feed disccells. The pH buffer 131 containing sodium bicarbonate neutralizeslactic acid 162, as shown in FIGS. 4-6, to relieve acid burn and backpain. In addition, the spiraled disc shunt 126 or spiraled filament 126halts progressive disc degeneration by stopping acidic hydrolysis of thedisc matrix, through pH normalization in the intervertebral disc 100. Inthe presence of oxygen 131, production of lactic acid 162 by disc cellsmay reduce, further relieving back pain. Nutrients 131 supplied throughspiraled disc shunt 126 feed disc cells to halt degradation ofproteoglycans for sugars and disc cell survival.

During relaxation of the intervertebral disc 100, the spiraled filament126 expands, as shown in FIG. 92, absorbing or drawing nutrient, oxygenand pH buffer 131 from the shallow endplate 105 diffusion into thespiraled filament 126. The spiraled filament 126 acts as a bridge,sponge or absorbent between superior and inferior endplate diffusionzones, conveying or distributing nutrient, oxygen and pH buffer 131through out the disc 100. Disc compression and relaxation from dailyactivities of the patient act as the pump for discharging and loadingnutrient, oxygen and pH buffer 131 from and into the spiral filament126.

Disc cells 277 isolated from advanced degenerated human discs 100 arestill capable of producing collagen and glycosaminoglycans in tissueculture with abundant supply of nutrients in proper pH. (Gruber H. E.,Leslie K., Ingram J., Hoelscher G., Norton H. J., Hanley E. N. Jr.:Colony formation and matrix production by human anulus cells: modulationin three-dimensional culture, Spine, July 1, 29(13), E267-274, 2004.Johnstone B, Bayliss M T: The large proteoglycans of the humanintervertebral disc, Changes in their biosynthesis and structure withage, topography, and pathology, Spine, March 15; 20(6):674-84, 1995.)Furthermore, stem cells have recently been found in degenerated discs.(Risbud M V, Gattapalli A, Tsai T T, Lee J Y, Danielson K G, Vaccaro AG, Albert T J, Garzit Z, Garzit D, Shapiro I M: Evidence for skeletalprogenitor cells in the degenerate human intervertebral disc, Spine,November 1; 32(23), 2537-2544, 2007.) Nutrient 131 deficiency and acidicpH may hinder disc 100 repair in-vivo.

The filament 126 or shunt 126 can be scaffolds and spigots for supplyingnutrients/oxygen/pH buffering solute 131 for cell 277 attachment, asshown in FIG. 42. With a continual or renewable supply ofnutrients/oxygen/pH buffer solutes 131, disc cells 277 resume makingbiosynthetic products 160, such as the water-retainingglycosaminoglycans and collagen, the major components of the nucleus 128and annulus 378. In sheep study, newly formed glycosaminoglycans onnylon strands 104 of the shunt 126 after 3 months can be seen usingSafranin histological staining.

The rate of sulfate incorporation for biosynthesizing glycosaminoglycansis pH sensitive. The maximum rate of sulfate incorporation is with pH7.2-6.9. The rate of sulfate incorporation drops about 32-40% in acidicpH within the disc [Ohshima H, Urban J P: The effect of lactate and pHon proteoglycan and protein synthesis rates in the intervertebral disc.Spine, September: 17(9), 1079-82, 1992]. Hence, pH normalization with pHbuffer solute 131 through the shunt 126 will likely increase productionof the water-retaining glycosaminoglycans and swelling pressure of theshunted disc 100.

With a continual supply of nutrients 131, newly formed biosyntheticproducts 160 increase osmolarity within the shunted disc 100 and enhanceinward fluid flow, as shown in FIGS. 40 and 42. The increased fluid flowcomes through (1) the external shunt 126, (2) blood capillaries 107through the endplates 105, and/or (3) annulus 378. The fluid is alsoretained by the newly formed water-retaining glycosaminoglycans 160. Asa result, the swelling pressure of the shunted disc 100 increases.Segmental or spinal instability is reduced. Muscle tension and ache fromguarding the spinal instability decrease. Load and pain of the facetjoints 129 decrease. Lactic acid 162 is further neutralized by inflow ofnutrients/oxygen/pH buffering solute 131 to reduce or alleviate acidburn. Disc 100 height is elevated, raised or increased as depicted byarrows in FIGS. 40-41. Implantation of the shunt 126 enables thedegenerated disc 100 to be repaired.

Furthermore, adenosine triphosphate, ATP, is the high-energy compoundessential for driving or energizing biochemical reactions, including thebiosynthesis of the water retaining glycosaminoglycans for sustainingcompressive loads on the disc 100. Under anaerobic conditions,metabolism of each glucose molecule produces only two ATP and two lacticacids 162, which irritate adjacent nerves 118. When oxygen 131 permeatesthrough the internal and/or external shunt 126, thirty-six ATP can beproduced from each glucose molecule through glycolysis, citric acidcycle and electron transport chain under aerobic conditions to energizedisc regeneration and alleviate back pain.

High concentration of nutrients 131 can also be injected into theinternal and/or external shunted disc 100 to instantly create highosmolarity, as shown in FIG. 43. High osmolarity promotes fluid inflowinto the shunted disc 100. However, glucose or sugars injection canproduce additional lactic acid 162, causing more pain. Sulfate and aminoacids can be injected in high concentration to boost osmolarity andproduction of glycosaminoglycans and collagen, as the biosyntheticproduct 160 in FIG. 42. Magnesium sulfate, potassium sulfate, or sodiumsulfate can be the injectable with high water solubility and isessential for biosynthesis of glycosaminoglycans in the nucleus pulposus128. Proline and glycine can also be injectables with high watersolubility and are essential nutrients 131 for biosynthesis of collagenin the annulus 378.

Analgesics, anti-depressant, steroid, NSAID, antibiotics,anti-inflammatory drugs, alkaline agent or other drugs can also beinjected into the shunted disc 100 to instantaneously reduce pain.

Autograft disc cells 277 from a healthy disc 100 of the patient can betransplanted into the degenerated and shunted disc 100 to promote discregeneration and production of biosynthetic product 160, as shown inFIG. 43.

The avascular disc 100 is well sealed and immuno-isolated. Even smallions, such as sulfate, and small molecules, such as proline, are greatlylimited from diffusing into the nucleus pulposus 128. The well sealeddisc 100 may be able to encapsulate donor cells 277 from a disc 100 ofanother person, cadaver or even animal without triggering an immuneresponse, and probably not needing anti-rejection drug. For disc 100regeneration, the donor cells 277 can also be stem cells 277, notochord277 or chondrocytes 277. The filament 126 or shunt 126 is permeable tonutrients/oxygen/pH buffering solute 131 but impermeable to cells and/orcytokines responsible for triggering an immune reaction. The cells ofthe immune system include giant cells, macrophages, mononuclearphagocyts, T-cells, B-cells, lymphocytes, Null cells, K cells, NK cellsand/or mask cells. The cytokines may also include immunoglobulins, IgM,IgD, IgG, IgE, other antibodies, interleukins, lymphokines, monokines orinterferons.

The molecular weights of nutrients 131 and lactic acid 162 are muchsmaller than the immuno-responsive cells and cytokines. The transportselectivity can be regulated or limited by the size of the pores orchannels within the semi-permeable shunt 126. The upper molecular weightcut-off of the shunt 126 can be 100,000 or lower to allow the passage ofnutrients and waste but exclude the immuno-responsive cells andcytokines. The semi-permeable shunt 126 may also contain ionic oraffinity surfaces to attract nutrients 131 and waste, including lacticacid 162. The surfaces of the semi-permeable shunt 126 can be made,coated or modified to repel, exclude or reject immuno-responsivecomponents.

In recent years, cell transplants from cadavers or live donors have beensuccessful in providing therapeutic benefits. For example, islet cellsfrom a donor pancreas are injected into a type I diabetic patient'sportal vein, leading into the liver. The islets begin to function asthey normally do in the pancreas by producing insulin to regulate bloodsugar. However, to keep the donor cells alive, the diabetic patientrequires a lifetime supply of anti-rejection medication, such ascyclosporin A. In addition to the cost of anti-rejection medication, theside effects of these immuno-suppressive drugs may include cancer. Thebenefit of cell transplant may not out weigh the potential side effects.

The shunted intervertebral disc 100 can be used as a semi-permeablecapsule to encapsulate the injected therapeutic donor cells 277 oragent, as shown in FIG. 43, to evade the immune response; hence nolife-long immuno-suppressive drug would be required. A variety of donorcells 277 or agent can be harvested and/or cultured from the pituitarygland (anterior, intermediate lobe or posterior), hypothalamus, adrenalgland, adrenal medulla, fat cells, thyroid, parathyroid, pancreas,testes, ovary, pineal gland, adrenal cortex, liver, renal cortex,kidney, thalamus, parathyroid gland, ovary, corpus luteum, placenta,small intestine, skin cells, stem cells, gene therapy, tissueengineering, cell culture, other gland or tissue. The donor cells 277are immunoisolated within the shunted discs 100, the largest avascularorgans in the body, maintained by nutrients/oxygen/pH buffer 131 andwaste transport through the shunt 126 or fissure 121. The donor cells277 can be from human, animal or cell culture. When disc pressure is lowduring sleep or supine position, nutrients/oxygen/pH buffering solutes131 are supplied through the shunt 126 to the donor cells 277. Duringwaking hours while the pressure within the disc 100 is high,biosynthesized products 160 by these donor cells 277 are expelledthrough the shunt 126 into the muscle 193 or through fissures 121 intobodily circulation and target sites.

The biosynthesized product 160 made by the donor cells 277 can beadrenaline, adrenocorticotropic hormone, aldosterone, androgens,angiotensinogen (angiotensin I and II), antidiuretic hormone,atrial-natriuretic peptide, calcitonin, calciferol, cholecalciferol,calcitriol, cholecystokinin, corticotropin-releasing hormone, cortisol,dehydroepiandrosterone, dopamine, endorphin, enkephalin, ergocalciferol,erythropoietin, follicle stimulating hormone, γ-aminobutyrate, gastrin,ghrelin, glucagon, glucocorticoids, gonadotropin-releasing hormone,growth hormone-releasing hormone, human chorionic gonadotrophin, humangrowth hormone, insulin, insulin-like growth factor, leptin, lipotropin,luteinizing hormone, melanocyte-stimulating hormone, melatonin,mineralocorticoids, neuropeptide Y, neurotransmitter, noradrenaline,oestrogens, oxytocin, parathyroid hormone, peptide, pregnenolone,progesterone, prolactin, pro-opiomelanocortin, PYY-336, renin, secretin,somatostatin, testosterone, thrombopoietin, thyroid-stimulating hormone,thyrotropin-releasing hormone, thyroxine, triiodothyronine, trophichormone, serotonin, vasopressin, or other therapeutic products. Thesebiosynthetic products 160 have low molecular weights and are able to betransported through the shunt 126 and/or fissures 121, while the donorcells 277 are trapped within the disc 100.

The biosynthesized products 160 (hormones, peptides, neurotransmitter,enzymes, catalysis or substrates) generated within the shunted disc 100may be able to regulate bodily functions including blood pressure,energy, neuro-activity, metabolism, and activation and suppression ofgland activities. Some hormones and enzymes govern, influence or controleating habits and utilization of fat or carbohydrates. These hormones orenzymes may provide weight loss or gain benefits. Producingneurotransmitters, such as dopamine, adrenaline, noradrenaline,serotonin or γ-aminobutyrate, from the donor cells 277 within theshunted disc 100 can treat depression, Parkinson's disease, learningdisability, memory loss, attention deficit, behavioral problems, mentalor neuro-related diseases.

Release of the biosynthesized products 160 by the donor cells 277 withinthe shunted disc 100 is synchronized with body activity. Duringactivities of daily living, the pressure within the shunted disc 100 isusually high to expel the biosynthesized products 160 by the donor cells277 into circulation to meet the demands of the body. In the supineposition, pressure within the shunted disc 100 is low; fluid inflow 161through the shunt 126 is favorable, bringing nutrients/oxygen/pH buffer131 into the disc 100 to nourish the cells 277. As an example, islets ofLangerhans from a donor's pancreas can be implanted or injected into theshunted disc 100. In supine position during sleeping, glucose entersinto the shunted disc 100 to induce production of insulin from theimplanted islets of Langerhans. During waking hours when disc pressureis high, insulin is expelled through the shunts 126 or fissure 121 intocirculation to regulate concentration of glucose in the body. At night,the insulin released from the shunted disc 100 is minimal to preventhypoglycemia. In essence, biosynthesized products 160 by the donor cells277 are released concurrent with physical activity to meet the demandsof the body.

Donor cells 277 can also be seeded on the shunt 126 or injected days,weeks, months or even years after implanting the disc shunts 126, toensure favorable biological conditions, including pH, electrolyticbalance and nutrients and oxygen 131, for cell 277 survival andproliferation in the shunted disc 100.

In the United States, average age of patients undergoing back surgery isabout 40-45 years old. The disc shunt 126 is preferred to be made withpermanent material to provide long-lasting pain relief. A wide range ofnon-degradable materials can be used to fabricate the shunt 126.Polymers, such as nylon, polytetrafluoroethylene, polypropylene,polyethylene, polyamide, polyester, polyurethane, silicon,poly-ether-ether-ketone, acetal resin, polysulfone, polycarbonate, silk,cotton, or linen are possible candidates. Fiberglass can also be a partof the shunt strands 104, to provide capillarity for transportingnutrients 131 and waste.

Especially for investigative purposes, biodegradable shunts 126 mayprovide evidence within weeks or months. Since the disc shunt 126degrades within months, any unforeseen adverse outcome would bedissipated. If the investigative-degradable shunt 126 shows promise,permanent shunt 126 can then be implanted to provide continuousbenefits. The biodegradable shunt 126 can be made with polylactate,polyglycolic, poly-lactide-co-glycolide, polycaprolactone, trimethylenecarbonate, silk, catgut, collagen, poly-p-dioxanone or combinations ofthese materials. Other degradable polymers, such as polydioxanone,polyanhydride, trimethylene carbonate, poly-beta-hydroxybutyrate,polyhydroxyvalerate, poly-gama-ethyl-glutamate, poly-DTH-iminocarbonate,poly-bisphenol-A-iminocarbonate, poly-ortho-ester, polycyanoacrylate orpolyphosphazene can also be used.

The filament needle 101 and cannula 230 can be made with stainlesssteel, nickel-titanium alloy or other metal or alloy. The needle 101 andcannula 230 can be coated with lubricant, tissue sealant, analgesic,antibiotic, radiopaque, magnetic and/or echogenic agents.

The disc shunt 126 can be used as a drug delivery device, deliveringoral, intravenous or injectable drugs into the avascular or nearlyimpenetrable disc 100 to treat infection, inflammation, pain, tumor orother disease. Drugs can be injected into the muscle 193 to be drawninto the shunted disc 100. Discitis is a painful infection orinflammatory lesion in the intervertebral disc 100 of adults andchildren (Wenger D R, Bobechko W P, Gilday D L: The spectrum ofintervertebral disc-space infection in children, J. Bone Joint Surg.Am., 60:100-108, 1978. Shibayama M, Nagahara M, Kawase G, Fujiwara K,Kawaguchi Y, Mizutani J: New Needle Biopsy Technique for Lumbar PyogenicSpondylodiscitis, Spine, 1 November, Vol. 35-Issue 23, E1347-E1349,2010). Due to the avascular nature of the disc 100, oral or intravenousdrugs cannot easily reach the bacteria or inflammation within the disc100. Therefore, discitis is generally difficult to treat. However, thedisc shunt 126 can be used as a drug-delivery device. The disc shunt 126draws the systemic drugs from muscles 193 into the sealed, avasculardisc 100. In addition, antibiotics, anti-inflammatory drugs, anestheticsor other drugs can be injected into the muscle 193 near the disc shunt126 to increase drug concentration within the disc 100 to treat discitisor pain. Injection near the shunt 126 is called peri-shunt injection.

Staphylococcus aureus is the most common bacteria found in discitis. Theshunt 126 can be loaded or coated with an antibiotic, such as nafcillin,cefazolin, dicloxacilin, clindamycin, bactrim, penicillin, mupirocin(bactroban), vancomycin, linezolid, rifampin,sulfamethoxazole-trimethoprim or other, to treat staphylococcus aureusinfection. Corynebacterium is also found in discitis. The shunt 126 canbe loaded or coated with an antibiotic, such as erythromycin,vancomycin, eifampin, penicillin or tetracycline, to treatcorynebacterium infection. Other antibiotics, such as cefdinir,metronidazole, tinidazole, cephamandole, latamoxef, cefoperazone,cefmenoxime, furazolidone or other, can also be used to coat the shunt126.

Inflammation in the disc 100 can cause excruciating pain. MRI can showinflammation at the endplates 105, and distinguish inflammatoryclassification as Modic I, II or III. The disc shunt 126 can be coatedor loaded with nonsteroidal anti-inflammatory drugs/analgesics (NSAID),such as aspirin, diflunisal, salsalate, ibuprofen, naproxen, fenoprofen,ketoprofen, flurbiprofen, oxaprozin, indomethacin, sulindac, etodolac,ketorolac, diclofenac, nabumetone, piroxicam, meloxicam, tenoxicam,droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid,flufenamic acid, tolfenamic acid, celecoxib, rofecoxib, valdecoxib,parecoxib, lumiracoxib, etoricoxib, firocoxib, nimesulide, licofelone orother NSAID, to treat inflammation in the disc 100 for pain relief.

The disc shunt 126 can also be coated or loaded with steroidalanti-inflammatory drugs/analgesics, such as betamethasone, budesonide,cortisone, dexamethasone, hydrocortisone, methylprednisolone,prednisolone, prednisone, triamcinolone or other steroid, to treatinflammation in the disc 100 for pain relief.

The shunt 126 can be loaded or coated with anesthetics, such asprocaine, amethocaine, cocaine, lidocaine, prilocalne, bupivacaine,levobupivacaine, ropivacaine, mepivacaine, dibucaine, methohexital,thiopental, diazepam, lorazepam, midazolam, etomidate, ketamine,propofol, alfentanil, fentanyl, remifentanil, sufentanil, buprenorphine,butorphanol, diamorphine, hydromorphone, levophanol, meperidine,methadone, morphine, nalbuphine, oxycodone, oxymorphone, pentazocine orother anesthetic, to provide instant pain relief.

The shunt 126 can be loaded or coated with a muscle relaxant, such assuccinylcholine, decamethonium, mivacurium, rapacuronium, atracurium,cisatracurium, rocuronium, vecuronium, alcuronium, doxacurium,gallamine, metocurine, pancuronium, pipecuronium, tubocurarine or otherrelaxant, to relieve muscle tension and ache.

The shunt 126 can be loaded or coated with buffering agents, such assodium carbonate, sodium bicarbonate, potassium carbonate, potassiumbicarbonate, magnesium carbonate, calcium carbonate, barium carbonate,potassium phosphate, sodium phosphate or other buffering agent, toneutralize lactic acid 162 and spontaneously alleviate pain caused byacid irritation or burn.

The shunt 126 can be loaded or coated with alkaline agents, such asmagnesium oxide, magnesium hydroxide, sodium hydroxide, potassiumhydroxide, barium hydroxide, cesium hydroxide, strontium hydroxide,calcium hydroxide, lithium hydroxide, rubidium hydroxide, neutral aminesor other alkaline agent, to neutralize lactic acid 162 and spontaneouslyalleviate pain caused by acid irritation.

The shunt 126 can be loaded or coated with initial supplies of nutrients131, such as sulfate, glucose, glucuronic acid, galactose,galactosamine, glucosamine, hydroxylysine, hydroxylproline, serine,threonine, chondroitin sulfate, keratan sulfate, hyaluronate, magnesiumtrisilicate, magnesium mesotrisilicate, magnesium oxide, magnosil,orthosilicic acid, magnesium trisilicate pentahydrate, sodiummetasilicate, silanolates, silanol group, sialic acid, silicic acid,boron, boric acid, other mineral, other amino acid or nutrients 131, toenhance or initiate production of sulfated glycosaminoglycans andcollagen within the degenerative disc 100.

Oral intake of antidepressants has shown temporary pain reduction orpain tolerance in back pain patients. Anti-depressants can be coated onthe shunt 126 to treat chronic back pain. The anti-depressant coatingmay include tricyclic antidepressant, serotonin-reuptake inhibitor,norepinephrine reuptake inhibitor, serotonin-norepinephrine reuptakeinhibitor, noradrenergic/serotonergic antidepressants,norepinephrine-dopamine reuptake inhibitor, serotonin reuptakeenhancers, norepinephrine-dopamine disinhibitors or monoamine oxidaseinhibitor. The antidepressant can be amitriptyline, amitriptylinoxide,butriptyline, clomipramine, demexiptiline, desipramine, dibenzepin,dimetacrine, dosulepin/dothiepin, doxepin, duloxetine, imipramine,imipraminoxide, lofepramine, melitracen, metapramine, nitroxazepine,nortriptyline, noxiptiline, pipofezine, propizepine, protriptyline,quinupramine, amineptine, iprindole, opipramol, tianeptine,trimipramine, or other antidepressant.

Fibrous formation over the shunt 126 may affect the exchange ofnutrients 131 and waste between the disc 100 and bodily circulation ormuscle 193. Immuno inhibitor can be coated or incorporated into theshunt 126 to minimize fibrous formation or tissue response. Examples ofimmuno inhibitors include but are not limited to: actinomycin-D,aminopterin, azathioprine, chlorambucil, corticosteroids, crosslinkedpolyethylene glycol, cyclophosphamide, cyclosporin A, 6-mercaptopurine,methylprednisolone, methotrexate, niridazole, oxisuran, paclitaxel,polyethylene glycol, prednisolone, prednisone, procarbazine,prostaglandin, prostaglandin E₁, sirolimus, steroids or other immunesuppressant drugs.

The shunt 126 can be loaded or coated with a calcium channel blocker forinhibiting activation of neuro-receptor to alleviate pain. The calciumchannel blocker can be dihydropyridines, phenylalkylamines,benzothiazepines, magnesium ion, Amlodipine, Felodipine, Isradipine,Lacidipine, Lercanidipine, Nicardipine, Nifedipine, Nimodipine,Nisoldipine, Verapamil, Diltiazem or other calcium channel blocker.

Healthy intervertebral discs 100 are avascular. To ensure avascularconditions, the shunt 126 can be incorporated, coated or partiallycoated with an anti-angiogenic compound. Examples of anti-angiogeniccompounds include, but are not limited to, Marimastat from BritishBiotech [a synthetic inhibitor of matrix metalloproteinases (MMPs)], Bay12-9566 from Bayer (a synthetic inhibitor of tumor growth), AG3340 fromAgouron (a synthetic MMP inhibitor), CGS 27023A from Novartis (asynthetic MMP inhibitor), COL-3 from Collagenex (a synthetic MMPinhibitor, Tetracycline® derivative), Neovastat from Aeterna, Sainte-Foy(a naturally occurring MMP inhibitor), BMS-275291 from Bristol-MyersSquib (a synthetic MMP inhibitor), TNP-470 from TAP Pharmaceuticals, (asynthetic analogue of fumagillin; inhibits endothelial cell growth),Thalidomide from Celgene (targets VEGF, bFGF), Squalamine from MagaininPharmaceuticals (Extract from dogfish shark liver; inhibitssodium-hydrogen exchanger, NHE3), Combretastatin A-4 (CA4P) fromOxigene, (induction of apoptosis in proliferating endothelial cells),Endostatin collagen XVIII fragment from EntreMed (an inhibition ofendothelial cells), Anti-VEGF Antibody from Genentech, [Monoclonalantibody to vascular endothelial growth factor (VEGF)], SU5416 fromSugen (blocks VEGF receptor signaling), SU6668 from Sugen (blocks VEGF,FGF, and EGF receptor signaling), PTK787/ZK 22584 from Novartis (blocksVEGF receptor signaling), Interferon-alpha (inhibition of bFGF and VEGFproduction), Interferon-alpha (inhibition of bFGF and VEGF production),EMD121974 from Merck, KcgaA (small molecule blocker of integrin presenton endothelial cell surface), CAI from NCl (inhibitor of calciuminflux), Interleukin-12 from Genetics Institute (Up-regulation ofinterferon gamma and IP-10), IM862 from Cytran, Avastin, Celebrex,Erbitux, Herceptin, Iressa, Taxol, Velcade, TNP-470, CM101,Carboxyamido-triazole, Anti-neoplastic urinary protein, Isotretionin,Interferon-alpha, Tamoxifen, Tecogalan combrestatin, Squalamine,Cyclophosphamide, Angiostatin, Platelet factor-4, Anginex, Eponemycin,Epoxomicin, Epoxy-β-aminoketone, Antiangiogenic antithrombin III,Canstatin, Cartilage-derived inhibitor, CD59 complement fragment,Fibronectin fragment, Gro-beta, Heparinases, heparin hexasaccharidefragment, Human chorinonic gonadotropin, Interferon (alpha, beta orgamma), Interferon inducible protein (IP-10), Interleukin-12 (IL-12),Kringle 5 (plasminogen fragment), Tissue inhibitors ofmetalloproteinases, 2-Methoxyestradiol (Panzem), Placental ribonucleaseinhibitor, Plasminogen activator inhibitor, Prolactin 16 kD fragment,Retinoids, Tetrahydrocortisol-S, Thrombospondin-1, Transforming growthfactor beta, Vasculostatin, and Vasostatin (calreticulin fragment).

The shunt 126 can be loaded or coated with lactic acid inhibitor orlactate dehydrogenase inhibitor. The lactic acid inhibitor or lactatedehydrogenase inhibitor includes fluoropyruvic acid, fluoropyruvate,levulinic acid, levulinate, oxamic acid, N-substituted oxamic acids,oxamate, oxalic acid, oxalate, beta-bromopropionate,beta-chloropropionate, malonate, sodium formaldehyde bisufite,chloroacetic acid, alpha-chloropropionate, alpha-bromopropionate,beta-iodopropionate, acrylate, acetoin, malic acid, glycolate,diglycolate, acetamide, acetaldehyde, acetylmercaptoacetic acid, alphaketobutyrate, thioglycolic acid, nicotinic acid, alpha-ketoglutarate,butanedione, hydroxypyruvic, chloropyruvic, bromopyruvic,2,3-dihydroxy-6-methyl-4-(1-methylethyl)-1-naphthoic acid, diethylpyrocarbonate, hexyl N,N-diethyloxamate, 3-acetylpyridine adeninedinucleotide, 7-p-Trifluoromethylbenzyl-8-deoxyhemigossylic acid,dihydroxynaphthoic acids, N-substituted oxamic acids, gossypol, gossyliciminolactone, derivatives of gossypol, dihydroxynaphthoic acid,2,3-dihydroxy-6-methyl-4-(1-methylethyl)-1-naphthoic acid, blue dye,reactive blue dye #2 (Cibacron Blue 3G-A) urea, methylurea and hydantoicacid, glyoxylate, hydroxybutyrate, 4-hydroxyquinoline-2-3 carboxylicacids, sodium bisulfate, dieldrin, L-(+) beta monofluorolactic acid,fluoro-lactic acid, tartronic acid, mesotartarate, sesquiterpene8-deoxyhemigossylic acid(2,3-dihydroxy-6-methyl-4-(1-methylethyl)-1-naphthoic acid), oranalogues of these chemicals.

In summary, the disc shunt 126 alleviates back pain by (1) drawingnutrients/oxygen/pH buffer 131 into the disc 100, (2) neutralizinglactic acid 162 to alleviate acid burn, (3) converting anaerobic toaerobic conditions to reduce lactic acid 162 production, (4) increasingsulfate incorporation in neutral pH for biosynthesis ofglycosaminoglycans. (5) increasing ATP production from aerobicmetabolism of sugars to drive biosynthetic reactions in disc 100, (6)bulking up the disc 100 to take load off painful facet joints 129, (7)fortifying the disc 100 to reduce spinal instability and muscle tension,(8) rebuilding disc matrix to increase osmolarity, fluid intake andabsorption, (9) re-establishing the swelling pressure to sustain disc100 compression, (10) regenerating the disc 100 for long term painrelief, and/or (11) delivering systemic drugs in disc 100 to treatdiscitis.

Unlike many surgical interventions of the spine, benefits of the discshunt 126 include (1) spinal motion preservation, (2) no tissue removal,(3) reversible by extraction, (4) micro-invasive, (5) out-patientprocedure, (6) approved implant material, (7) 15-minutes per disc, (8)long-lasting and no-harm-done, (9) no incision, (10) compatible withdrugs, conservative treatment or surgical intervention, if needed, and(11) drug coated shunt if needed to expedite pain relief.

The present invention of the shunt 126 or filament 126 is spirallyformed distal to a needle 101 and cannula 230, packing into a disc 100,reaching one or both diffusion zones 106A, 106B between 0 and 3 mm fromthe endplates 105, to draw nutrients/oxygen/pH buffer 131 diffused fromcapillaries 107 at the endplate 105 into the mid layer of the disc 100.Nutrients and cells 277 can be intradiscally injected for discregeneration and/or production of biosynthetic product 160.

It is to be understood that the present invention is by no means limitedto the particular constructions disclosed herein and/or shown in thedrawings, but also includes any other modification, changes orequivalents within the scope of the claims. Many features have beenlisted with particular configurations, curvatures, options, andembodiments. Any one or more of the features described may be added toor combined with any of the other embodiments or other standard devicesto create alternate combinations and embodiments. A pH electrode may beexposed near the tip of the needle 101 to detect the acidity within thedisc 100.

It should be clear to one skilled in the art that the currentembodiments, materials, constructions, methods, tissues or incisionsites are not the only uses for which the invention may be used.Different materials, constructions, methods or designs for varioussections 126A, 126B and 126C can be substituted and used. The disc shunt126 can be called a filament, strand, thread, line, conduit, wick,sponge or absorbent. Spiraled shunt 126 can be called a coiled shunt orcoiled filament 126. The snagging point 231 can be called the snagger231. The filament gripper 111 can be called the gripper 111. Nothing inthe preceding description should be taken to limit the scope of thepresent invention. The full scope of the invention is to be determinedby the appended claims.

What is claimed is:
 1. A deployment device for implanting a selectableamount of filament within a tissue, the deployment device comprising: acannula capable of being guided such that a distal tip thereof may belocated within an implant location of the tissue, a preformed helicalfilament comprises a proximal portion and a distal portion, wherein saidpreformed helical filament further comprises a helical position and astraightened position, a filament needle comprises a proximal end, adistal end, and a lumen, wherein said distal portion of said preformedhelical filament is in said straightened position in said lumen, saiddistal end of said filament needle and said distal portion of saidpreformed helical filament locatable within said cannula, said distalportion of said preformed helical filament is capable of being advancedgenerally parallel and distal to said filament needle, thereby saiddistal portion of said preformed helical filament resumes said helicalposition in the implant location, and said filament needle is capable ofbeing rotated, thereby spiraling said helical position of said preformedhelical filament into a predetermined spiral in the implant location. 2.A deployment device for implanting a selectable amount of filamentwithin a tissue, the deployment device comprising: a needle capable ofreaching and puncturing into an implant location of the tissue, a guidewire comprises a distal length insertable into said needle, a dilatorcomprises a longitudinal opening sized to slide over said guide wire, acannula comprises a longitudinal channel sized to slide along saiddilator, wherein said cannula further comprises a distal tip, apreformed helical filament comprises a proximal portion and a distalportion, wherein said preformed helical filament further comprises ahelical position and a straightened position, a filament needlecomprises a proximal end, a distal end and a lumen, wherein said distalportion of said preformed helical filament is in said straightenedposition in said lumen, said distal end of said filament needle and saiddistal portion of said preformed helical filament locatable within saidcannula, said distal portion of said preformed helical filament iscapable of being advanced generally parallel and distal to said filamentneedle, thereby said distal portion resumes said helical position ofsaid preformed helical filament, and said filament needle is capable ofbeing rotated, thereby spiraling said preformed helical position of saidpreformed helical filament into a predetermined spiral in the implantlocation.
 3. The deployment device of claim 1 or 2, wherein saidfilament needle is capable of being advanced, rotated and retracted morethan once, thereby allowing said deployment device to pack multiple saidpredetermined spirals of said preformed helical filament in the implantlocation.
 4. The deployment device of claim 1 or 2 further comprises anone-way filament retainer in said cannula, wherein said one-way filamentretainer comprises at least one filament snagger sized and configured toengage at least a portion of said preformed helical filament.
 5. Thedeployment device of claim 4, wherein said at least one filament snaggertakes a form of a pointed tip.
 6. The deployment device of claim 4,wherein said one-way filament retainer has a ribbon or curved shape. 7.The deployment device of claim 1 or 2, wherein said distal end of saidfilament needle comprises at least one filament gripper.
 8. Thedeployment device of claim 7, wherein said at least one filament grippertakes a form of a pointing tip.
 9. The deployment device of claim 1 or2, wherein said cannula comprises an elastic curvature.
 10. Thedeployment device of claim 1 or 2, wherein said filament needle iselastic.
 11. The deployment device of claim 1 or 2, wherein said cannulacomprises a proximal section, and wherein said proximal section furthercomprises a funnel.
 12. The deployment device of claim 11, wherein saidproximal section of said cannula further comprises a latch engaging saidproximal end of said filament needle.
 13. The deployment device of claim1 or 2, wherein said proximal end of said filament needle comprises abobbin, and wherein said proximal portion of said preformed helicalfilament is spooled over said bobbin.